Promethease results. Buy a DNA kit here: https://bit.
Promethease results. Promethease is an educational tool, it's fun to look at all the rare variants you might have. com data are different from both of these. SNPedia is a wiki-styled genetic data repository. For example, here is a sample report they link to on their homepage that uses 23andme data. 0, AncestryDNA, and FTDNA results. e. You can upload multiple data files to the same report to compare your results from different DNA Sep 11, 2018 · The rs code (or “rsID”) identifies a location for that genetic finding in the genome (the entire stretch of someone’s full DNA sequence, including all of the chromosomes). Oct 6, 2020 · How to read Promethease results? Promethease reports are based on SNPedia, a Wikipedia-styled repository. May 10, 2019 · Promethease and your privacy. A place for discussing Promethease, a report about your DNA based on the scientific I am a 31F adoptee who was curious about genetic diseases, so I decided to plug my 23andme raw data into Promethease. Note the frequencies on the last six are all extremely large cross-sections of the population, often majorities. ” Test results from Promethease shows themselves to be responsible service providers by ensuring participants are aware of where and how to use and interpret their results. My reported lowered risk is almost entirely due to my having two copies of APOE2. Though popular, it is often criticized for being too technical and difficult to read. (magnitude 4. Increased and Decreased Risk for Alzheimer’s. Oct 20, 2021 · Promethease is a DNA analysis service that provides information on your health risks based on your genetic makeup. And the results from my ancestry. g. My 23andme dna kit results in Promethease were pretty accurate. Mar 18, 2024 · On the Promethease website, the first thing you will see are the terms and conditions. Join group. Clicking on this part of the Promethease results will take you to a SNPedia article which highlights the research related to this variation, as well as links to the direct studies. Promethease retrieves all relevant literature from the SNPedia database. I need some help understanding my Promethease results. Carefully review before accepting these terms. Thank you so much. I think if you spend the time to read through it all, you'll probably find some good insights. Still I do understand that generally you can't draw too much of a conclusion about anything from this. ) use Promethease to retrieve Promethease — a tool for anyone to understand genetic health risks Promethease is a literature retrieval system that pulls its information from SNPedia, a vast wiki of research studies on how What is Promethease? Promethease is an online tool that analyzes raw DNA data. It is used by Promethease to create a personal report linking your DNA variations to the information This last weekend I was using my wife's ancestry DNA and uploading it to some sites like genetic genie, and promethease to see what they said. When looking at the frequency is a higher # better or worse than a lower # and just because I have the gene does that mean I'll get the condition? The results for the breast cancer are alarming at best. Hello! I recently ran my 23andme code through both Promethease and genetic genie, and they gave me dissimilar results. Were these results to be fed back to individuals, the clinical implications would be profound. The report also uses scientific language and jargon like SNP, allele, genotype, or rsID. To use this platform, you need to have access to your raw DNA data from another DNA testing company, as they don’t offer DNA tests. DNA testing can be used for genetic genealogy, but your DNA results can also be used to understand your health based on genetics. Hi all, I have a question about how to interpret my promethease result. I used to be a part of the network of genetic counselors at Genome Medical, thus I know and respect the policies they set surrounding DTC testing and raw data. As an added bonus, you can start a 30-day free trial of MyHer I have Hashimoto disease, i take a pill every morning of Levothyroxin. I'm also going to include markers associated with ADHD as I'm interested in learning about the links between them. Should I still have some of the results clarified? - rs6025 3. Sometimes, different codes One of the first impressions of the Promethease report is its sheer volume of data. I've been looking through my genes and the following are those I have that are associated with Autism. promethease. Aug 17, 2022 · “Promethease is a literature retrieval system that builds a personal DNA report based on connecting a file of DNA genotypes to the scientific findings cited in SNPedia. Some of the studies are free to access, while others you will have to access through a library or research institution with a subscription. 0 means it was not observed in a sample of 120 people. Promethease is a literature retrieval system that builds a personal DNA report based on connecting a file of DNA genotypes to the scientific findings. I have a BRCA test and mammogram concerning a lump next week. Buy a DNA kit here: https://bit. 1. Biomedical researchers, healthcare practitioners, and customers of DNA testing services such as 23andMe and AncestryDNA use Promethease to retrieve information published about their DNA variations. Such a pretty amazing and accurate results Jul 2, 2018 · Companies like Promethease warn customers not to regard their results as medical diagnoses. 5x as other members reported. A place for discussing Promethease, a report about your DNA based on the… Promethease gave quite a bit more info--the problem is you get too many hits with Promethease, and sometimes they are contradictory (e. My highest trait/disease magnitude is Hashimoto disease 11. Promethease provides results that fall into 3 categories: Bad – red Jan 28, 2019 · Promethease is a computer program developed by the SNPedia team which allows users to compare personal genomics results against the SNPedia database, generating a report with information about a person's attributes, such as propensity to diseases, based on the presence of specific single-nucleotide polymorphisms (SNPs) within their genome. Promethease generates a report using genetic information found on SNPedia. About this group. I just "might" have a story that is a real life example of what this 'atypical' BuChE association means for us? Here it is - in the late 90's, my mother went in to have surgery to get her carotid artery "cleaned" out - a rather involved, yet common procedure, as I understood. I have two insights so far: Paracetamol instead of Ibuprofen and watch out for thrombosis (long flights or in case I break my foot or leg). Jan 5, 2017 · A Promethease Report lists some basic information in a "header" at the top. 7. Jun 28, 2019 · The raw data that is uploaded to Promethease only includes the data from the SNPs tested by the original company. I am glad I purchased it, especially since it's so cheap. One nice feature of the service is that you can view some sample reports without uploading your raw data. com website and the ClinVar database. if one gene gives a 1. ” imgur pic Jan 17, 2024 · Unless you have a science or genetics background, Promethease is a less user friendly LiveWello. . But be aware that it requires you to upload your genetic data from a source like 23andme, so you need that first. com. The more red in color, the more rare this genotype. I used 23andMe dna data into promethease. Likewise, a Promethease DNA report compiles all of the genetic variants found in your genetic data. (i. How to get your raw data. Although Promethease provides a short tutorial at the beginning of each report, the tool is less polished or intuitive than those provided by other well-known genome analysis services. Personally, I'm conflicted. The terms and conditions include statements acknowledging the risk of learning about potential health conditions and the importance of consulting a healthcare professional for a better understanding of your Aug 21, 2020 · The amount of agency Promethease offers users in navigating their report results is impressive. com and get started already! May 26, 2023 · Promethease allows users to analyze their genetic data and compare personal genomics results against the SNPedia database. com): Overview: This website matches your 23 and Me, AncestryDNA, or other genetic data to the information on the Snpedia. It can feel overwhelming if you are new to genetics. I just found out that the promethease report only covers around 25,000 of the SNPs from 23andme. If you’re looking for a high level of detail and the ability to filter, organize, and compare test results, Promethease may be a good choice. These videos are getting quite old, but still offers some helpful information about reading a Promethease report. However, learning to navigate this interface can be difficult. For instance I have a variant in about 2% of the population which decreases the chance of male pattern baldness and otosclerosis, while increasing heart disease: rs1800472. For colorblind usersː In Promethease you can change the colors of your Promethease report to improve legibility. Jun 30, 2014 · As you’ll see, my original results from 23andMe are different from the Promethease results I get from the same 23andMe data. The majority ones should really be interpreted the other way around; you have the risk of (say) 60% of people, the baseline, and a significant minority have a lower risk. I was told four years ago I had dry macular degeneration and the results say I have 5. Review of Promethease (www. I too have the 'atypical' BuChE result on promethease. An associated computer program called Promethease, also developed by the SNPedia team, allows users to compare personal genetics results against the SNPedia database, generating a report with information about a person's attributes, such as propensity to diseases, based on the presence of specific SNPs within their genome. Interested in asking questions or discussing results with a genetic counselor? See Find a genetic counselor. simultaneous higher and lower risk for breast cancer). Promethease is a DNA tool that creates a genetic health report for you based on your DNA. First, while the results of the Promethease report are based on serious clinical studies and research, future findings may prove these results premature or incorrect so do not take them as absolute truth. Promethease accepts data uploads from several testing companies, including: AncestryDNA; 23andMe; Family Tree DNA I used 23andme to sequence my DNA which covers 600,000 SNPs. The following are my results from Promethease. This is a support sub for those with Ehlers-Danlos syndrome (all types) and HSD—diagnosed or waiting to be diagnosed. And there you have it! Remember to reach out to a genetic counselor if you found some unsettling information or are unsure of your results. Many Promethease users find that running a new report every 6 - 12 months tends to produce something new of interest compared to their last report, so that's at least one way to keep up to date with new findings. 161) and a time stamp when the report was generated. 78x increase, does having both of them give a much greater risk for the disease than just one? My Promethease Results upvotes · comments. I compared 23andMe, Geno 2. It uses an uncurated database of research on genetic variations to give you information on certain health traits and your genetic risk for various diseases. Let me know in the comments below whether that was helpful, or if you have any questions about how to decipher your Promethease results. ly/UsefulChartsDNAUse the coupon code GETDNA for free shipping. eu), Impute. This is a welcoming place for those affected (or those simply wanting to learn more) to ask questions, share successes and failures, feel less alone, and discuss everyday life. Dec 30, 2013 · I have been planning to blog on my results from Promethease. 4x risk of thrombosis See discussion at Rs6025. I will need to research directly on 23andme and update my post with all the Genotypes I actually have for each gene. I found Promethease worth the $5. Why is that and which should I rely on going forward? Oct 19, 2014 · Gene Results. ClinVar is a publicly accessible database that is managed by the National Institutes of Health (NIH) and tends to provide more reliable and robust results. As a final test, I combined all of my non-imputed files into one run in order to compare all of my non-imputed results, together, with DNA. Land’s imputed results. 10 DNA Upload Websites You Can Use Now (Including Free Sites) For example, each site and different test kit services use different datasets and algorithms to analyze your genetic ancestry, so you should try them and see if you can confirm your ethnicity estimate results, or it could discover a missing ethnicity that your original test did not show (e. me, Varsome and Enlis Genomics software. Odds ratio based on 2013 and 2017 studies. The results can also be downloaded as a zip file and opened in any web browser. SNPedia only had 43 Genotypes listed for SYNGAP1 gene. I just got my results from Promethease a couple of days ago. rs7158782(G;G) 4x higher risk of adverse side-effect if taking aromatase inhibitor rs7158782 is one of 4 SNPs found on chromosome 14 near a gene known as T-cell leukemia/lymphoma 1A ( TCL1A). These file formats are understood. Biomedical researchers, healthcare practitioners and customers of DNA testing services (such as 23andMe , Ancestry. 5-4. Am I interpreting these results correctly? Also, do multiple genes tend to stack? I. Promethease can reanalyze the results of genotype tests sold legally for $99 to $199 by a variety of genealogy companies, including 23andMe, Ancestry. Then, it allows you the tools to research the scientific papers which have reported results about specific variants you carry. Dec 30, 2023 · A Few Words of Warning Before Using Promethease. In one case, 23andMe gave me 1. Also bad for developing ankylosing spondylitis and was told I had that around 15 years ago. SNPedia is essentially a Wiki for Aug 26, 2024 · Promethease result for breast cancer How to Filter and Search the Report Promethease uses a wiki-style format , allowing you to search for specific genes, variants, or conditions of interest, similar to how you would use Wikipedia. As far as promethease goes I just want a quick result first, I understand its far from perfect being a machine generated report but it seems worth the $12. It provides the results as an online table that can be searched. This takes around 15 minutes. I am trying to figure out if I am “positive” for HLA-B27 and could possibly have Ankylosing Spondylitis. Promethease seems like the best available deal in personalized genetic medicine today. not many people have this genotype). r/promethease. Most reports on Promethease cost $12. Second, many sections of your health report are explained in multipliers based on averages. A Promethease Report lists some basic information in a "header" at the top. Promethease - DNA Results. The number is a percentage in your chosen population. 44x higher risk factor based on one study. I saw a lot of upsetting results, but the result that upset me the most was that I carry 7 different indicators that I'm at increased risk of developing multiple sclerosis. In other words, your results are based on specific regions of your DNA rather than the entirety of your genetic profile. Using 23andMe health results and comparing them to Promethease, Promethease looked at a lot more SNPs than 23andMe. The report is organized in a single rs ID format. com , FamilyTreeDNA , Genos , etc. I have always suspected that I have mild androgen insensitivity syndrome, I am a trans woman who was assigned male at birth and I have had very late puberty onset with basically no secondary sex characteristics development despite the fact that hormone levels tests I took before starting hormone replacement therapy have shown that I have insanely high testosterone levels (above the highest Jul 19, 2017 · SNPedia is a wiki investigating human genetics. 55x increase risk and another gives 1. Or go straight to promethease. 0. Price: $12 – $16 11 votes, 12 comments. Here, Kelli explains Promethease and shows us parts of her own DNA health report to demonstrate how useful Promethease can be. Once you have accepted the terms and conditions, you are presented with a video to watch. The ClinVar setting of your Promethease report allows you to filter your results based on genetic variants that are clinically associated with certain diseases. Different databases are available that track and use that rs code and compile all the information available about that particular variant. I work in the medical field as a nurse and I felt like the results were somewhat complicated to understand even coming from a medical background. However, if you’re just starting your ancestry research and are asking questions like “What is a haplogroup,” this service may not provide the information necessary to build a family tree and Oct 8, 2017 · Promethease results are color coded with red being a probable pathogenic result (meaning potentially concerning, or bad), green being a good or protective result and grey meaning not assigned as bad or good – just information. Women with a positive BRCA result face a lifetime of additional screening and potentially prophylactic surgery that is unwarranted in the case of a false positive result. 9 x chance of it so spot on. The purpose of this group is to engage in discussions about health- and trait-related DNA reporting and data Oct 11, 2017 · Promethease provides a wonderful feature that enables users to combine multiple vendors’ files into one run. However, we would argue that the GenVue Discovery platform and user experience is unrivaled and completely different than any other tools. com, and National Geographic’s I'm reading my report and apparently I'm an unwell person, or will be when I'm old. Promethease is a literature retrieval system that builds a personal DNA report based on connecting a file of DNA genotypes to the scientific findings cited in SNPedia. 8K subscribers in the promethease community. Promethease report is text-based with limited visuals, which can be challenging to read for the uninitiated. Promethease is one service that can create Sep 16, 2021 · Promethease is a DNA analysis service that provides a personalized health report based on your unique genetic makeup. , Genomelink, MyHeritage, LivingDNA). 1) GenVue Discovery by Genetic Genie is a free Promethease alternative, as well as an alternative to Codegen (codegen. My Google fu is failing me as to whether this is saying I am “positive. The results consist of information about a person’s risk of disease as well as information about traits. Please edit this page and leave your own questions. Jul 7, 2018 · You might also find Talk:Promethease helpful as well as Promethease/results. , Version 0. We share information about the effects of variations in DNA, citing peer-reviewed scientific publications. Mostly, they are comparing a consumer’s raw data to gene variants reported to be linked to disease. The first two lines show the version of Promethease that was run (e. Feb 25, 2018 · Conflict of interest declaration: I do not profit if any testing company receives business as a result of what I say or write. gyu aqumcgt swzivu ydu yfsoeb qjyqm ynwzzey ozzhs awywjo cckkr