C/CPublished research associates this genotype with typical/baseline likelihood of Fibrinogen — no copies of the reported risk allele. (GWAS Catalog, Arterioscler Thromb Vasc Biol 2011, PMID:21757653)
C/TPublished research associates this genotype (one copy of the reported risk allele) with an intermediate association with Fibrinogen. (GWAS Catalog, Arterioscler Thromb Vasc Biol 2011, PMID:21757653)
T/TPublished research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Fibrinogen compared to the general population. (GWAS Catalog, Arterioscler Thromb Vasc Biol 2011, PMID:21757653)
Arteriosclerosis, thrombosis, and vascular biology · 2011 · PMID 21757653
Questions about rs7681423
What is rs7681423?
rs7681423 is a single position in the genome, in or near the FGG gene. Published research associates it with fibrinogen. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs7681423 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 rs7681423 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 rs7681423 come from?
GWAS Catalog, Arterioscler Thromb Vasc Biol 2011, PMID:21757653. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.