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Who was studied 77,690 European ancestry cases, 1,167,040 European ancestry controls, 67,864 Japanese ancestry cases, 1,026,594 Japanese ancestry controls.
The effect
Each copy of the T allele shifted the measure 0.049 lower (95% confidence interval 0.036-0.062); p = 2 × 10−14.
How common The T allele had a frequency of about 29% in the people studied.
Where it sits Chromosome 6, band 6p22.3 — in an intron of ATXN1.
What each result means
C/CNo copy of the version the research linked to Atrial fibrillation. This is the starting point the study compared everyone against.
C/TOne copy of the version the research linked to Atrial fibrillation. That is a smaller link than two copies.
T/TTwo copies of the version the research linked to Atrial fibrillation. That is the strongest link of the three results. A link in a study is not a diagnosis.
Nature genetics · 2023 · PMID 36653681 · open access
Questions about rs9370893
What is rs9370893?
rs9370893 is a single position in the genome, in or near the ATXN1 gene. Published research associates it with 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 rs9370893 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 rs9370893 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 rs9370893 come from?
GWAS Catalog, Nature genetics 2023, PMID:36653681. 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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