3 4942334223125Reads by AI crawlersClaude4ChatGPT2Google · Gemini3Perplexity3Meta AI4Microsoft · Copilot2Amazon2Apple3China (ByteDance, Huawei, Baidu…)1ByteDance (Doubao)1Others25Total49Counted 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 13,105 African American individuals.
The effect
Each copy of the A allele shifted the measure 2.06 lower (95% confidence interval 1.43-2.69); p = 2 × 10−10.
How common The A allele had a frequency of about 25% in the people studied.
Where it sits Chromosome 1, band 1q24.2 — between genes, 0 kb from LOC101928596.
What each result means
A/ATwo copies of the version the research linked to QT interval. That is the strongest link of the three results. A link in a study is not a diagnosis.
A/GOne copy of the version the research linked to QT interval. That is a smaller link than two copies.
G/GNo copy of the version the research linked to QT 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 rs1320976
What is rs1320976?
rs1320976 is a single position in the genome, in or near the ATP1B1 gene. Published research associates it with qt 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 rs1320976 linked to?
On MyGeneLog this position is linked to QT Interval and Drug-Induced Long QT. The research behind each link, and its sources, are set out on that condition page.
What do people read about alongside rs1320976?
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 rs1320976 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 rs1320976 come from?
GWAS Catalog, Circ Cardiovasc Genet 2012, PMID:23166209. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
3 4942334223125Reads by AI crawlersClaude4ChatGPT2Google · Gemini3Perplexity3Meta AI4Microsoft · Copilot2Amazon2Apple3China (ByteDance, Huawei, Baidu…)1ByteDance (Doubao)1Others25Total49Counted 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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