Standard
HDL cholesterol
CD36 · rs2366858
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 HDL cholesterol — no copies of the reported risk allele.
A/C
Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with HDL cholesterol.
C/C
Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of HDL cholesterol compared to the general population.
Source
Genome-wide characterization of shared and distinct genetic components that influence blood lipid levels in ethnically diverse human populations
Coram MA,
Duan Q,
Hoffmann TJ,
Thornton T,
Knowles JW,
Johnson NA,
Ochs-Balcom HM,
Donlon TA,
Martin LW,
Eaton CB,
Robinson JG,
Risch NJ
and 5 more — show all
American journal of human genetics · 2013 · PMID 23726366
Questions about rs2366858
What is rs2366858?
rs2366858 is a single position in the genome, in or near the CD36 gene. Published research associates it with hdl cholesterol. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs2366858 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 rs2366858 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.
← See all variants