A/APublished research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Triglycerides compared to the general population. (GWAS Catalog, Circ Cardiovasc Genet 2015, PMID:26582766)
A/GPublished research associates this genotype (one copy of the reported risk allele) with an intermediate association with Triglycerides. (GWAS Catalog, Circ Cardiovasc Genet 2015, PMID:26582766)
G/GPublished research associates this genotype with typical/baseline likelihood of Triglycerides — no copies of the reported risk allele. (GWAS Catalog, Circ Cardiovasc Genet 2015, PMID:26582766)
rs1260333 is a single position in the genome, in or near the GCKR gene. Published research associates it with triglycerides. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs1260333 linked to?
On MyGeneLog this position is linked to High Triglycerides. The research behind each link, and its sources, are set out on that condition page.
Does having rs1260333 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 rs1260333 come from?
GWAS Catalog, Circ Cardiovasc Genet 2015, PMID:26582766. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.