0 313218123110Reads by AI crawlersClaude3ChatGPT2Google · Gemini0Perplexity1Meta AI8Microsoft · Copilot1Amazon2Apple3China (ByteDance, Huawei, Baidu…)1ByteDance (Doubao)1Others10Total31Counted 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 672 Korean ancestry cases, 3,700 Korean ancestry controls; replicated in 200 Korean ancestry cases, 1,812 Korean ancestry controls.
The effect
Each copy of the C allele carried 1.51 times the odds of Early onset atrial fibrillation (95% confidence interval 1.35-1.68); p = 1 × 10−12.
How common The C allele had a frequency of about 42% in the people studied.
Where it sits Chromosome 4, band 4q34.1 — inside HAND2-AS1.
What each result means
C/CTwo copies of the version the research linked to Early onset 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 Early onset atrial fibrillation. That is a smaller link than two copies.
T/TNo copy of the version the research linked to Early onset atrial fibrillation. This is the starting point the study compared everyone against.
rs4615152 is a single position in the genome, in or near the HAND2 gene. Published research associates it with early onset 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 rs4615152 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.
Does having rs4615152 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 rs4615152 come from?
GWAS Catalog, Eur Heart J 2017, PMID:28460022. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
0 313218123110Reads by AI crawlersClaude3ChatGPT2Google · Gemini0Perplexity1Meta AI8Microsoft · Copilot1Amazon2Apple3China (ByteDance, Huawei, Baidu…)1ByteDance (Doubao)1Others10Total31Counted 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.
Early onset atrial fibrillation (rs4615152). MyGeneLog™. https://www.mygenelog.com/variants/rs4615152