A/APublished research associates this genotype with typical/baseline likelihood of LDL cholesterol — no copies of the reported risk allele.
A/GPublished research associates this genotype (one copy of the reported risk allele) with an intermediate association with LDL cholesterol.
G/GPublished research associates this genotype (two copies of the reported risk allele) with a higher likelihood of LDL cholesterol compared to the general population.
American journal of human genetics · 2013 · PMID 23726366
Questions about rs12713956
What is rs12713956?
rs12713956 is a single position in the genome, in or near the APOB gene. Published research associates it with ldl cholesterol. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs12713956 linked to?
On MyGeneLog this position is linked to Cholesterol (LDL, HDL and Total). The research behind each link, and its sources, are set out on that condition page.
Does having rs12713956 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 rs12713956 come from?
GWAS Catalog, Am J Hum Genet 2013, PMID:23726366. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.