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Coagulation factor levels

OBP2A · rs8176704

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

A/A Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Coagulation factor levels compared to the general population. (GWAS Catalog, Proc Natl Acad Sci U S A 2012, PMID:23267103)

A/G Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Coagulation factor levels. (GWAS Catalog, Proc Natl Acad Sci U S A 2012, PMID:23267103)

G/G Published research associates this genotype with typical/baseline likelihood of Coagulation factor levels — no copies of the reported risk allele. (GWAS Catalog, Proc Natl Acad Sci U S A 2012, PMID:23267103)

Source: GWAS Catalog, Proc Natl Acad Sci U S A 2012, PMID:23267103

Questions about rs8176704

What is rs8176704?

rs8176704 is a single position in the genome, in or near the OBP2A gene. Published research associates it with coagulation factor levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs8176704 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 rs8176704 come from?

GWAS Catalog, Proc Natl Acad Sci U S A 2012, PMID:23267103. 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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