Sensitive

Venous thromboembolism

F11 · rs4253399

Stands on its own. Nothing else here links to this position yet — but the page above is the point: what the research found, what each genotype means, and where it came from, in language you can read. Links to conditions, drugs and the senses appear automatically if we write them.

What each result means

G/G Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Venous thromboembolism compared to the general population. (GWAS Catalog, Genet Epidemiol 2013, PMID:23650146)

G/T Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Venous thromboembolism. (GWAS Catalog, Genet Epidemiol 2013, PMID:23650146)

T/T Published research associates this genotype with typical/baseline likelihood of Venous thromboembolism — no copies of the reported risk allele. (GWAS Catalog, Genet Epidemiol 2013, PMID:23650146)

Source: GWAS Catalog, Genet Epidemiol 2013, PMID:23650146

Questions about rs4253399

What is rs4253399?

rs4253399 is a single position in the genome, in or near the F11 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.

Does having rs4253399 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 rs4253399 come from?

GWAS Catalog, Genet Epidemiol 2013, PMID:23650146. 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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