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Who was studied 23,151 European ancestry cases, 553,439 European ancestry controls, 2,261 African American cases, 49,400 African American controls, 654 Hispanic cases, 21,214 Hispanic controls; replicated in 17,672 cases, 167,295 controls.
The effect
Each copy of the G allele carried 1.06 times the odds of Venous thromboembolism (95% confidence interval 1.04-1.08); p = 9 × 10−10.
How common The G allele had a frequency of about 30% in the people studied.
Where it sits Chromosome 14, band 14q32.12 — inside CATSPERB.
What each result means
A/ANo copy of the version the research linked to Venous thromboembolism. This is the starting point the study compared everyone against.
A/GOne copy of the version the research linked to Venous thromboembolism. That is a smaller link than two copies.
G/GTwo copies of the version the research linked to Venous thromboembolism. That is the strongest link of the three results. A link in a study is not a diagnosis.
Nature genetics · 2019 · PMID 31676865 · open access
Questions about rs57328376
What is rs57328376?
rs57328376 is a single position in the genome, in or near the CATSPERB gene. Published research associates it with venous thromboembolism. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs57328376 linked to?
On MyGeneLog this position is linked to Venous Thromboembolism. The research behind each link, and its sources, are set out on that condition page.
Does having rs57328376 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 rs57328376 come from?
GWAS Catalog, Nat Genet 2019, PMID:31676865. 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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