Standard

Anticoagulant levels

PROCR · rs867186

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 with typical/baseline likelihood of Anticoagulant levels — no copies of the reported risk allele. (GWAS Catalog, PLoS One 2011, PMID:22216198)

A/G Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Anticoagulant levels. (GWAS Catalog, PLoS One 2011, PMID:22216198)

G/G Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Anticoagulant levels compared to the general population. (GWAS Catalog, PLoS One 2011, PMID:22216198)

Source: GWAS Catalog, PLoS One 2011, PMID:22216198

Questions about rs867186

What is rs867186?

rs867186 is a single position in the genome, in or near the PROCR gene. Published research associates it with anticoagulant levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs867186 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 rs867186 come from?

GWAS Catalog, PLoS One 2011, PMID:22216198. 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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