G/GPublished research associates this genotype (two copies of the reported risk allele) with a higher likelihood of D-dimer levels compared to the general population.
G/TPublished research associates this genotype (one copy of the reported risk allele) with an intermediate association with D-dimer levels.
T/TPublished research associates this genotype with typical/baseline likelihood of D-dimer levels — no copies of the reported risk allele.
Papers in Europe PMC whose title or abstract names both this rsID and that subject. A shared paper means somebody wrote about the two together — it is not a claim that this position explains the subject.
Questions about rs12029080
What is rs12029080?
rs12029080 is a single position in the genome, in or near the F3 gene. Published research associates it with d-dimer levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs12029080 linked to?
On MyGeneLog this position is linked to Fibrinogen and Blood Clotting. The research behind each link, and its sources, are set out on that condition page.
What do people read about alongside rs12029080?
Subjects that appear in the title or abstract of the same papers as this rsID include brain and memory (1 papers). A shared paper means somebody wrote about the two together; it is not a claim that this position explains the topic.
Does having rs12029080 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 rs12029080 come from?
GWAS Catalog, Circulation 2011, PMID:21502573. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.