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Venous thromboembolism

F2 · rs1799963

Where this position leads

Condition: Venous Thromboembolism

rs1799963 Condition: Venous Thromboembolism Venous Thromboembolism Condition rs1799963 rs1799963 F2

What each result means

A/A Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Venous thromboembolism compared to the general population.
A/G Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Venous thromboembolism.
G/G Published research associates this genotype with typical/baseline likelihood of Venous thromboembolism — no copies of the reported risk allele.
Source
Genetic Analysis of Venous Thromboembolism in UK Biobank Identifies the ZFPM2 Locus and Implicates Obesity as a Causal Risk Factor
Klarin D, Emdin CA, Natarajan P, Conrad MF, Kathiresan S
INVENT Consortium
Circulation. Cardiovascular genetics · 2017 · PMID 28373160

Questions about rs1799963

What is rs1799963?

rs1799963 is a single position in the genome, in or near the F2 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 rs1799963 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 rs1799963 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 rs1799963 come from?

GWAS Catalog, Circ Cardiovasc Genet 2017, PMID:28373160. 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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