Promethease reddit.

Promethease reddit Not only did they NOT delete my data, they have now sold it. Posted by u/chongae - No votes and 2 comments A place for discussing Promethease, a report about your DNA based on the scientific literature cited in SNPedia. The Archive of Our Own (AO3) offers a noncommercial and nonprofit central hosting place for fanworks. A result that says “gene variation A gives you 1. I've been looking through my genes and the following are those I have that are associated with Autism. The interface is not so friendly, it is more functional, and I do not understand it. Im just saying you're complaining about something promethease was never meant or claim to do. If you have multiple such SNPs it will be higher but still nowhere near a "you will have MS" statement. just uploading raw data from Download your raw data from Ancestry, there’s a button or something to do it, and then upload the file to promethease. I've tried responding to the Processing Delay emails, and going to the Help/Contact section of Promethease. Sub-saharan Africans carry the R allele at a frequency of 40%. But on my personal report, I have 2 data files, one from Ancestry & one from 23andMe. I recently got my promethease report, and I inputted on the search bar Gs122. 1K subscribers in the promethease community. I re-downloaded the raw-file and it says II there too, but when I use their online raw data browser it says CC, and on promethease II. codegen. Examples are at the end. I have reports for my whole family on my promethease account and none of those populate a report. Is that true? So I guess it comes down to whether the extra cost of 23andMe health info on top of Promethease is worth it vs. My highest trait/disease magnitude is Hashimoto disease 11. This indicates that your promethease report has 6 snps which are linked to Thyroid cancer, 1 snp related to Torsion dystonia etc. Just like with everything, there are probably other risk factors that should be considered, environmental, etc. 5x prostate cancer ?! Are my results wrong? Genes linked to Autism Spectrum Conditions(ASC) There was a significant association between rs2268493 in OXTR and AS. I have done both of those and have several anxiety inducing possible miscalls that I hope the full genome sequencing will confirm or exclude for me. eu - a free promethease-ish service for ancestry testing raw data. We are proactive and innovative in protecting and defending our work from commercial exploitation and legal challenge. com) show gs246, which Promethease report describes as: "APOE E3/E3 Apo-ε3/ε3, the most common form of APOE. However, if you used promethease, you should just be able to search in their results (search for "celiac" and read through the results; there are a lot that simply contribute to the risk or not, but the DQ2/8 stuff should be in there as well). 4K subscribers in the promethease community. com. I have noticed that I carry several of the mutations that may be possibly linked to ADHD. Multiple haplotypes that include this SNP (rs2268493-rs2254298, rs2268490-rs2268493-rs2254298, rs2268493-rs2254298-rs53576, rs237885-rs2268490-rs2268493-rs2254298, rs2268490-rs2268493-rs2254298-rs53576) were also associated with AS. Have you taken the tutorial, and do you have questions about it? Please do so, and also read the /LearnMore pages because they should help you understand genetics a bit better before you jump to conclusions, and that's pretty essential to understanding any report about your DNA. Then I clicked that baldness tag and these popped up. We don't do any ancestry analysis; the information you get is "4th percentile of male pattern baldness" or "92nd percentile for risk tolerance," etc. Promethease takes your 23andMe data and shows it nicely formatted by gene etc, drawing directly on the snpedia database of research, I don't think it's making any judgements or interpretations of its own. Your Promethease report should have shown that CHEK2 mutation, which is known as rs555607708 to most of the world but is named i4000462 by 23andMe. So, any ideas what is happening!? Here is the stack : Traceback (most recent call last): 8. That individual SNPs don't matter one at the time in diseases such as Crohn's (or any other common disease for that matter) In addition, Promethease is a "look up table" that looks into public databases to see if there is any information about the meaning of the variant. Promethease is only $12 but it's a one-time cost and you can keep running reports every so often as the science advances. Personally, my Promethease report showed a high(ish) magnitude to a type of cancer that I was later diagnosed and treated for. Promethease If you choose not to create an account. Regardless of all the well meaning explanations of magnitude - ok, I guess ultimately they point to the same thing. Apparently it's pretty rare with a frequency of just 2. A good thing with Promethease is that it gives some sources for you to explore further if you want. This lead down a rabbit hole on how to create small . The first three are characterized as bad with "Greatly/substantially increased odds of developing V617F-positive MPN" TLDR; GPT is shockingly good at genetic analysis, especially when given access to formatted data and some simple tools. The magnitude 3. It seems this reddit is so controlled by pro-promethease people, that it's almost impossible to write anything negative about them without getting kicked to the end of the stack. vcf files from . I have an appointment tomorrow to discuss this with my PCP after my rheumatologist recommended following up with him. 7. A place for discussing Promethease, a report about your DNA based on the scientific literature cited… >54x higher risk of schizophrenia, 5. Schizophrenia - Promethease. Members Online Understanding DNA results for Alzheimer's For rs4420638 I have the A;G variant, which Promethease tell's me give me a 3x chance of developing Alzheimer's. Promethease is much more difficult to understand but I strongly suggest it. ] [Sometimes it will wind up in a spam folder rather than your inbox. They kept my newest combined file at least. We see these calls with high frequency in Ancestry. So we paid for a website that is showing wrong datas, and not really what is in our raw data. So I plugged my data into Promethease. If you find anything worth digging into, make sure that SNP isn't on the conflict list and always reference it against nebula's information to ensure accuracy using this method. com data. Does that mean I have the bad ApoE e4 variant? I also have rs5882(G;G), which is associated with a 70% lower risk of Alzheimer's. I emailed them at all of the possible emails (the old ones and the ones from myheritage). com when your report is ready. Both Genie and Prom correctly picked up my carrier status for a common recessive condition, but both missed the second (rarer) disease for which I’m also a carrier 🤷‍♂️ Quoting the Promethease author's post in a closed Facebook group for Dante and Nebula: I'm the author of Promethease, and I now have a new thing which is designed from scratch for WGS (& WES). I am pissed about it! Did a test through 23andme, but can't find my ABO type So I went to Promthease, and it shows: ABO blood type unknown rs8176719(I;D) rs8176746(A;C) rs8176747(C;G) 7. It is of course it is possible that that someone actually does have the true mutation, but data from Ancestry is useless for determining it, because the noise swamps the signal. I wish to make analyze my DNA for (rare diseases), with Nebula Genomics (WGS 100x). Promethease's magnitude value helps a bit with this as very damaging variants for which there is a lot of evidence for pathogenicity should have higher magnitude scores. MAOA is an enzyme involved in the degradation of some neurotransmitters. Some users found that their genetic information had been acquired by MyHeritage despite their attempts to delete it from the Promethease databases. 4x bipolar, 21x thyroid cancer, 18x testicular cancer, 6. Its just telling you those studies are there. com (no longer accepting uploads Promethease on the other hand is just a long list of mutually inconsistent reports on weak effect SNPs. See full list on selfhack. The conversation about Promethease on Twitter You also need to consider the evidence that is being used to claim an increased risk of MS. Much of the Tutorial offered when your Promethease report first opens if all about how to search, sort, filter and order your report, and tip #16 in particular mentions how to print or export summaries from your report in CSV, Excel and PDF formats. And the evidence for rs1805086 is very conclusive if you look at it logically. i might be able to give more insight if i had more of your symptoms The sprint gene you're referring to is called ACTN3. Anything above magnitude 3 might be worth paying attention to. com data to be harmful. They both take you to a blank wiki. [Sometimes it will wind up in a spam folder rather than your inbox. Members Online Very new on this journey and feeling extremely overwhelmed. 2 things could be equally bad, but one of them has an easy treatment ('eat more Leutine'), because there are actions you can take, we'd give that one a higher magnitude. NutraHacker and Genetic Genie were the most helpful to me regarding nootropics. We prioritize privacy above all else. Jul 19, 2024 · Promethease is by far the best third-party data analysis tool, but there are many others out there to choose from. They stated specifically that this would not happen, and i only used their service because of this promise. 7%, so that doesn't make me feel better! We would like to show you a description here but the site won’t allow us. From what I understand, they only check for 5 of the 500+ known Pompe Disease mutations on the GAA gene, and 2 or more of those 500+ mutations would indicate being affected instead of just a carrier. 1, with 4. that's how some intersex people discover they're not XX female. Ignore promethease, it’s a waste of your time. The only thing that came up was rs1160312(A;A). I took the 23andme genetic test and put my raw data through promethease and it returned 4 different markers for ADHD, which is… Anyways, which one should I trust more. (Note that Promethease reports from Ancestry data will not return accurate ApoE status due to lack of relevant data. A place for discussing Promethease, a report about your DNA based on the scientific literature cited… A place for discussing Promethease, a report about your DNA based on the scientific literature cited in SNPedia. But you will probably get a few nebulous results from miscalls, but it's pretty accurate as is and is the least effort. We would like to show you a description here but the site won’t allow us. For example thats how they transfer all of their data from Promethease to MyHeritage after the company acquisition. Members Online Gene expression identical twins MAOA 3 repeat version? You can use the vcf directly on promethease, which is probably the easiest for health identification. I thought that the $30 was well worth it. Or you can leave your data with Promethease. Or check it out in the app stores Promethease. My daughter's file is gone and so are my older files. Livewello - 20 dollars for for various reports generated from ancestry raw data files. 1 being the highest I could go). Hi, I got my Promethease report with my AncestryDNA data. We also offer whole genome sequencing, the most advanced genetic test. My dad has all three of them so I felt a little shocked by its accuracy. com Jul 5, 2022 · Promethease predicts disease risks from uploaded DNA data, but results can be difficult to understand. They are way too common in Ancestry. My 23andme dna kit results in Promethease were pretty accurate. Gotten a r/promethease: A place for discussing Promethease, a report about your DNA based on the scientific literature cited in SNPedia. gencove. Which DNA test is best to upload to Promethease of 23andMe, Ancestry, and MyHeritage? I already uploaded FTDNA in 2018, but now I intend to upload… Average risk for MS (at least for the US) is 0,35%. I think it's important to note that there will be conflicts detected, but these conflicts should be listed by promethease. A place for discussing Promethease, a report about your DNA based on the scientific literature cited… Hi, I just got my DNA sequenced through 23 and me and I have 94. Anything at 3 or lower are mostly curiosities. Promethease is a great tool if you want to investigate your genes further! You can upload your 23andme raw data and it will cross reference your tested alleles with their database of genetics literature. I know it's pretty common to get a lot of bad results, but what freaked me out most was a 3. I could relate to your animal snack comments; I didn't like beheading animal crackers at all! Get the Reddit app Scan this QR code to download the app now. Promethease have lied. Promethease is slightly more reliable, but there’s a fee yet there is virtually no customer service to show for it. Members Online Question about rs1801181 - Diagnosed with Ehlers Danlos Syndrome Hi. Promethease has it sorted it so that your highest magnitude stuff appears at the top of the report. )" "23andMe Both the $99 "ancestry only" product and the $199 "ancestry + health" product are useable with Promethease, and the raw data is identical from both products and therefore results in exactly the same Promethease report I recently received a new report on my 23&Me account notifying me that I am a carrier for Pompe Disease. In other words, it means that SNP is normal and you likely do not carry any CYP2D6*3 alleles. SNPedia says to post questions here. Since you say you have Rs35742686(I;I) on Promethease, that means I can ignore orientation issues, so that corresponds to the Rs35742686(A;A) entry on the Rs35742686 page. Those are the most relevant (and usually most well-studied) SNPs. It's ambitious, trying to be high end. Family history in description. You can't use Promethease to analyse a complex disease like Crohn's. 8. Back in 2020 I have taken a 23andMe genetic test and have today used its raw data to generate a Promethease report. "Low activity MAO-A could significantly predict aggressive behaviour in a high provocation situation, but was less associated with aggression in a low provocation situation" Using Promethease, I had the results rs12340895(G;G), rs3780374(A;A), rs10974944(G;G) and rs77375493(G;G). If you entered your email address correctly, you will receive an email from reports@promethease. If you mention this reddit post or DM me you'll get a 70-80% discount. It's early and I'm looking for early adopters. If you're talking about the MAOA gene, it's on the X chromosome, so if you're male you can't get it from your dad and need to get it from your mom. It's hard to read a lot of meaning into magnitude. By the way, many Promethease reports have no genotypes of magnitude higher than 4. 5 times more likelihood of suffering from X” comes from a group study where a thousand people get sequenced and rare variation A is more common in people with X. It doesn't save your file like Promethease does. Also just know that Ancestry seems to give a lot of weird misscalls with Promethease, so if some rare genetic disorder/disease shows up just know it may just be A place for discussing SNPedia, a curated wiki about human DNA variants and the source for Promethease reports. I don't want to go to my doctor looking like a hypochondriac if these are insignificant and the number of them, for different genes, makes me think they probably are actually miscalls. Feb 4, 2019 · Promethease — a tool for anyone to understand genetic health risks; 3 filter suggestions for your report; Breakdown of terminology; 3 easy ways to sort your filtered report; My raw data is the same as when I was first uploaded it, but all of a sudden this is appearing at the top of my Promethease results. 4 certainly isn't earth shaking. However I am fairly sure it is better than 23&me which looks pretty but not much else. As the title indicates, 23andme claims that there's a 74% chance that I will NOT experience male pattern baldness (MPB) prior to the age of 40 (and a 26% chance I will). Also its an Isreali company with in itself is kinda sketchy. 2). It is considered the "neutral" genotype, with E2 having lower risk and E4 having higher risk of Alzheimer's disease. 4x risk of thrombosis (magnitude 4. It is not meant to be a post-peer review tool of those same studies. Oh - and please do up-vote if you see this. Promethease ranks this slightly higher in Magnitude (2. 7K subscribers in the promethease community. Reddit users have expressed serious concerns about the validity of Promethease’s commitments to privacy. This reports is made based on data from SNPedia, which contains ~200 SNPs tagged with schizophrenia. Each report using its respective data file from Ancestry. So it's good to hear from an AA's perspective. If you have a SNP that increases your risk 3-fold that would still be about 1%. I've now had access to Promethease results for many members of my family, along with a couple of friends and we were all AG. comments sorted by Best Top New Controversial Q&A Add a Comment The following are my results from Promethease. bam files and that would require a huge investment of time. I have results post-FDA-ban, and I'm not sure how the old data compares to Promethease. 5 suggests that this is a minor risk. Now, the 23andme data is very much the opposite of the Promethease data with regards to heart and cancer risks, even things like cilantro-tasting are all re Promethease isnt using any of these studies to claim anything. Get the Reddit app Scan this QR code to download the app now A place for discussing Promethease, a report about your DNA based on the scientific literature cited When you uploaded it to Promethease did you also upload any other tests like Ancestry or 23andme. (Completely made up examples) If you live under powerlines in a high pesticide farm and are a heavy alcoholic, your risk might be an additional 5-10X the normal risk as well. The fact is that your data is at risk no matter where it is. Somebody mentioned Promethease to me but I have just taken a look and there is some controversy as apparently they "sold out" to the genealogy company myheritage. 18 votes, 11 comments. For each of these SNPs, the Promethease curated report will tell you if you have the common or the risk variant. It is considered to be responsible for borderline personality disorder because of its role in aggression, general anxiety disorder, impulsivity, and mood lability. rs2180439 (C:C) - reduced risk of MPB rs2003046 (C:C) - Normal (higher) risk of MPB rs8085664 (C;C) - normal (higher) risk of MPB rs6625163 (A;A) - increased risk of baldness rs2073963 (G;G) - increased risk of baldness rs1160312 (G;G) - reduced risk of baldness rs1385699 (T;T That’s what promethease said with a note it might be more serious with another genes involvement. Are there any other services that offer similar things like Promethease? Also has anyone requested their data analyzed by promethease lately? I've been waiting for 2 days when they said it was going to take 20 mins. Selfdecode is more interpretive, they have staff drafting reports. It's isn't the most pretty or user friendly but it does a reasonable job for the price. If you decide to create the account they reserve the rights to share your data with their partners. A place for discussing Promethease, a report about your DNA based on the scientific literature cited… Posted by u/AbsoluteNerve - 5 votes and 5 comments Jul 5, 2022 · User reviews of Promethease on Reddit compare Promethease to Xcode Life. So I put in my dna to promethease to view my balding gene risk and saw that pretty much every single one was negative, but on 23andme, it said I had… I uploaded my dna to promethease, it says I'm female. you can just look at the raw data and see if there is a y chromosome to confirm. Promethease is by far the best third-party data analysis tool, but there are many others out there to choose from. So I downloaded my raw data from myheritage and uploaded it to promethease and found that I'm a carrier of this gene : rs4307059 (T;T) (magnitude : 3 ) The promethease report seems to be legitimate, found out I may develop type 2 diabetes,prostate cancer,baldness. Instead, they will likely be replaced by much more limited, and much pricier, pre-approved reports designed for the general consumer that cover on Hi - I did the 23andMe and it said I was not at risk for balding. I tried recently to upload my . 26 votes, 11 comments. The problem is that we know these databases are wrong ~25% of the time. My apoE results (raw data from Ancestry. There is a bit of a learning curve but once toy spend hours reading through it and SNPedia, you will get far more out of it then anything else 23andme could offer. Reply reply A place for discussing Promethease, a report about your DNA based on the scientific literature cited in SNPedia. ] Yes, I think Genetic Life Hacks is the most useful one I have used, including Promethease, Genetic Genie, and Nutrahacker. They will match any format against a bunch of different databases and produce a report that should be much more complete than promethease considering the price. very little of the genome was actually surveyed), it can also mean that the person isn't carrying a known, "nasty" genotype such as one often leading to an unwanted medical condition; in other An unofficial sub devoted to AO3. Imho it's rather expensive. I’ll put it simply - if you have to go on a bulletin board to ask about what a gene variant means, then you are NOT equipped to deal with the data. You can then decide if you want to go forward to do further more directed testing. its just weird how I could have near-guaranteed levels of no balding on 23andme and really bad results on promethease Dec 9, 2021 · Also in 2019, Reddit users reported that MyHeritage gained access to their raw genetic data from Promethease even after they deleted their information. I have been working in the genomics and diagnostics industry for over 25 years and in my opinion the Promethease service is simply unethical. I didn't get anything outlandish so I'm not really worried about false Jul 19, 2024 · If you're interested in getting more health-related info out of your data, Promethease is a tool that may be of interest. They are unequivocally scam artists. Note that this particular mutation is linked to a somewhat more moderate (~2-5 perhaps) increase in risk for breast cancer than are the more pathogenic BRCA1 and BRCA2 mutations, but does also have some other cancer risks as you mentioned. The expert said it isn’t a straightforward Disease like that and full gene testing would need to be done which I didn’t do. just uploading raw data from A place for discussing Promethease, a report about your DNA based on the scientific literature cited in SNPedia. I'm leaning more towards 23andme just because they compared my dna with other people but I'm not too sure now. Members Online rs1801181 (t;t) and Ehlers Danlos/sulfur Note that this file used to work, and I had a report from Promethease last year. Every time you want a print out or to read it you have to resubmit but the entire process took about five minutes. eu is a decent free alternative to Promethease that gives you much of the same information. A place for discussing Promethease, a report about your DNA based on the scientific literature cited… Open menu Open navigation Go to Reddit Home Hello! Can anyone help me understand whether I can determine if I have a COMT mutation through my Promethease report? I am able to pull up some… Correct. While I understand that you can upload the 23andMe info to Promethease, I heard that a Promethease report based on Ancestry raw data contains more than twice as many genotypes as 23andMe. Let me know if you need any more help. 5-4. I do agree with your idea of holding reddit for 8. There you will find the information you seek, though I can't help you as far as interpretation goes. Mine came up with the same variants but gave them different weights in terms of how they might affect me. e. Everyone has lots of these polymorphic variants that slightly increase or decrease your risk to develop various health concerns, but you cannot interpret any of them in isolation and even a well-validated polygenic risk score isn’t going to tell your actual risk with any level of certainty. 1 vs. Hey that's me. Promethease reports while a lot of data will give you a magnitude report that is quite detailed. Read more in our Promethease review! Feb 4, 2019 · Today I’m showing you how to make the most out of your Promethease report, by giving you suggestions on how to filter and sort it to produce the easiest, most digestible report. 6K subscribers in the promethease community. 7% middle-eastern heritage (to be expected). 9K subscribers in the promethease community. Schizophrenia is found as a part of the standard curated Promethease report in medical conditions. Would love any suggestions! Aug 21, 2020 · The conversation about Promethease on Reddit . 63 votes, 50 comments. rs2268493 has been previously associated with Promethease combines results from heaps of studies around the world. I also have EDS and have taken genetics courses, unfortunately because EDS is relatively newly accepted and with the exception of vascular type of EDS (which effects the arteries and veins) and classical (which causes you to have extremely loose and stretchy skin) the most common type of EDS, hypermobility type does not yet have a known genetic cause. can also check sry and ar genes plus there is list of conditions on the right you can scroll through. I than put the results into Promethease. But, here's the thing that gets me, when i look up this specific gene variant on any other gene site, it says its on the y chromosome and not the x like promethease says, so I'm really confused as to whether or not i have a y chromosome or if I'm just missing an x A place for discussing Promethease, a report about your DNA based on the scientific literature cited in SNPedia. I'm also going to include markers associated with ADHD as I'm interested in learning about the links between them. I'm going to a genetic counselor in a few weeks to get tested again, but I want to know if I can trust my Promethease results for the most part. A place for discussing Promethease, a report about your DNA based on the scientific literature cited… I tested with Ancestry and according to Promethease it was indeed the v2c version. A place for discussing Promethease, a report about your DNA based on the… Promethease should call two genosets for CYP2D6, just use those. Interesting! They say it is specifically aggression when triggered, situational aggression. The two main ones being: rs1801131(A;C) Possibly impaired folate metabolism - MTHFR rs1801131 (C) or MTHFR A1298C Posted by u/420dankmemes1337 - 8 votes and 10 comments A few years ago 23andme was better for promethease because even though it tests less snps than ancestry (neither of them are close to a complete sequence), it tested more of the medically relevant ones. Okay, fine, i am/was afab. the results indicate multiple SPNs with "higher risk" for developing the MPN. Because Promeathease has been taken over by MyHeritage, I surmise that the cheap reports they offer may disappear. It costs $12 if I remember correctly. Such a pretty amazing and accurate results A place for discussing Promethease, a report about your DNA based on the scientific literature cited in SNPedia. To put it bluntly, my DNA information was stolen by promethease and sold to a company. But i don't understand if Promethease will read my VCF or BAM… In order to better sort data Promethease has "magnitude" as an indicator. I happened to come across my promethease results 4 years after my initial Raw data was uploaded. I've seen that AncestryDNA and Promethease are both fairly accurate. Nebula Genomics. 23andme, or Promethease. Promethease was showing the wrong alleles and the Genetic genie was showing the right alelles. A place for discussing Promethease, a report about your DNA based on the… May 10, 2019 · Making a Promethease report; Reading a Promethease report; Sample Promethease reports from a person tested on different 23andMe DNA chip versions: 23andMe v4 (2014) 23andMe v3 (2011) 23andMe v1 (2008) Sample Promethease reports for another person based on data from different companies (23andMe, FamilyTreeDNA): 23andMe v3; FamilyTreeDNA. Nebula Genomics stands out compared to other genomic health reporting services. I dont care what you have to say about promethease. Although this can mean the raw data isn't very comprehensive (i. The UI is slightly better. Promethease clearly indicates I have SNPs on the X Chromosome that are pro-balding. It enhances Promethease in my opinion. The more places you upload it, the more places it will be at risk. It does say I have some other deletions in the COL5A1 gene, but not what I can find in any other EDS associated gene. A place for discussing Promethease, a report about your DNA based on the scientific literature cited… I'd go with the promethease report. Go figure. 5x as other members reported. A place for discussing Promethease, a report about your DNA based on the scientific literature cited in SNPedia. There are magnitude=4 genotypes which are good. No files > 4GB are supported. bam and it posted a message that the file format was not supported. Promethease and 23andMe Health Alternative The good news is that Promethease and 23andMe can be complementary services – you can use your raw DNA data from 23andMe to access Promethease’s One of the pages in the promethease report you can download shows a looong list of conditions, and there are red and green bars next to each that show your relative risk based on all of the SNPs related to each condition and whether each increases or decreases your risk. You should probably ask in r/promethease, r/genetics, r/23andme or r/AncestryDNA, since you're asking a question about health-related aspects of genetic testing, whereas this sub would be more appropriate if your question was related to genetic genealogy. Genetic Life Hacks was the only one that flagged a fairly rare gene variant that was causing my chronic cough (Alha-1 Antitrypsin Deficiency). And there are a lot more. The bar shows you how many of those snps are classified as having Good (green), Unknown (Grey) or Bad (Red) Repute . I feel comfortable with Promethease's attempts to protect the data, but as we have seen with the US Government and Equifax, nobody's data is completely safe, no matter where My wife and I both have all the same things showing for MTHFR. MH who bought their main source of data called "SNPpedia" and censored some of the data in that database reducing the types of reports they can be made. fpoczn ebano ubhvgh jfem nsnx qqehp jvfxibt yduhz pnqffm cso