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Who was studied 212,199 European ancestry individuals.
The effect
Each copy of the A allele shifted the measure 0.0206 higher (95% confidence interval 0.014-0.027); p = 3 × 10−10.
How common The A allele had a frequency of about 63% in the people studied.
Where it sits Chromosome 12, band 12q13.11 — in a non-coding transcript of SLC38A4-AS1.
What each result means
A/ATwo copies of the version the research linked to QRS duration. 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 QRS duration. That is a smaller link than two copies.
G/GNo copy of the version the research linked to QRS duration. This is the starting point the study compared everyone against.
Nature communications · 2022 · PMID 36050321 · open access
Questions about rs7976280
What is rs7976280?
rs7976280 is a single position in the genome, in or near the SLC38A4-AS1 gene. Published research associates it with qrs duration. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs7976280 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.
Does having rs7976280 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 rs7976280 come from?
GWAS Catalog, Nature communications 2022, PMID:36050321. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
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