5 443233222324Reads by AI crawlersClaude3ChatGPT2Google · Gemini0Perplexity3Meta AI3Microsoft · Copilot2Amazon2Apple2China (ByteDance, Huawei, Baidu…)3ByteDance (Doubao)3Others24Total44Counted 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 28,517 European ancestry individuals.
The effect
Each copy of the C allele shifted the measure 1.49 ms lower (95% confidence interval 1.08-1.90); p = 9 × 10−13.
How common The C allele had a frequency of about 40% in the people studied.
Where it sits Chromosome 5, band 5q35.1 — between genes, 0.8 kb from Y_RNA.
What each result means
C/CTwo copies of the version the research linked to PR interval. 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 PR interval. That is a smaller link than two copies.
T/TNo copy of the version the research linked to PR interval. 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 rs251253
What is rs251253?
rs251253 is a single position in the genome, in or near the NKX2-5 gene. Published research associates it with pr interval. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs251253 linked to?
On MyGeneLog this position is linked to Cardiac Conduction Intervals (PR Interval and QRS Duration). The research behind each link, and its sources, are set out on that condition page.
What do people read about alongside rs251253?
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 rs251253 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 rs251253 come from?
GWAS Catalog, Nat Genet 2010, PMID:20062060. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
5 443233222324Reads by AI crawlersClaude3ChatGPT2Google · Gemini0Perplexity3Meta AI3Microsoft · Copilot2Amazon2Apple2China (ByteDance, Huawei, Baidu…)3ByteDance (Doubao)3Others24Total44Counted 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.
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