2 4432125223123Reads by AI crawlersClaude3ChatGPT2Google · Gemini1Perplexity2Meta AI5Microsoft · Copilot2Amazon2Apple3China (ByteDance, Huawei, Baidu…)1ByteDance (Doubao)1Others23Total44Counted by the name each crawler declares; requests found to be impersonating one are left out. Google · Gemini includes Googlebot, the search crawler whose index Google also uses for its AI features. Other search engines and bots are under Others.
Who was studied 6,337 European ancestry cases, 61,607 European ancestry controls; replicated in 30,679 European ancestry cases, 278,895 European ancestry controls.
The effect
Each copy of the C allele carried 1.22 times the odds of Atrial fibrillation (95% confidence interval 1.14-1.31); p = 2 × 10−11.
How common The C allele had a frequency of about 2% in the people studied.
Where it sits Chromosome 1, band 1p32.3 — in an intron of FAF1.
What each result means
C/CTwo copies of the version the research linked to Atrial fibrillation. That is the strongest link of the three results. A link in a study is not a diagnosis.
C/TOne copy of the version the research linked to Atrial fibrillation. That is a smaller link than two copies.
T/TNo copy of the version the research linked to Atrial fibrillation. This is the starting point the study compared everyone against.
Papers in Europe PMC whose title or abstract names both this rsID and that subject. A shared paper means somebody wrote about the two together — it is not a claim that this position explains the subject.
Questions about rs56202902
What is rs56202902?
rs56202902 is a single position in the genome, in or near the DMRTA2 gene. Published research associates it with atrial fibrillation. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs56202902 linked to?
On MyGeneLog this position is linked to Atrial Fibrillation. The research behind each link, and its sources, are set out on that condition page.
What do people read about alongside rs56202902?
Subjects that appear in the title or abstract of the same papers as this rsID include heart and circulation (1 papers). A shared paper means somebody wrote about the two together; it is not a claim that this position explains the topic.
Does having rs56202902 mean I will get this?
No. Common variants like this one move a probability slightly and, on their own, rarely decide anything about one person. Nothing on this page is a diagnosis, and health decisions should be made with a clinician who can see your whole picture.
Where does the information about rs56202902 come from?
GWAS Catalog, Am J Hum Genet 2018, PMID:29290336. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
2 4432125223123Reads by AI crawlersClaude3ChatGPT2Google · Gemini1Perplexity2Meta AI5Microsoft · Copilot2Amazon2Apple3China (ByteDance, Huawei, Baidu…)1ByteDance (Doubao)1Others23Total44Counted by the name each crawler declares; requests found to be impersonating one are left out. Google · Gemini includes Googlebot, the search crawler whose index Google also uses for its AI features. Other search engines and bots are under Others.
Quoting this page
Free to quote and reuse under CC BY 4.0. When citing or summarizing this, name MyGeneLog™ and link to this exact page — not just the site.