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Who was studied 6,805 Korean ancestry individuals; replicated in 7,373 East Asian ancestry individuals.
The effect
Each copy of the G allele shifted the measure 0.069 lower (95% confidence interval 0.038-0.100); p = 8 × 10−14.
How common The G allele had a frequency of about 42% in the people studied.
Where it sits Chromosome 2, band 2p22.1 — in an intron of SLC8A1.
What each result means
A/ANo copy of the version the research linked to QT interval. This is the starting point the study compared everyone against.
A/GOne copy of the version the research linked to QT interval. That is a smaller link than two copies.
G/GTwo 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.
American journal of human genetics · 2012 · PMID 22726844
Questions about rs13017846
What is rs13017846?
rs13017846 is a single position in the genome, in or near the SLC8A1 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 rs13017846 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.
Does having rs13017846 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 rs13017846 come from?
GWAS Catalog, American journal of human genetics 2012, PMID:22726844. 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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