CD36 · rs75326924
Where this position leads
Condition: Hypo-HDL-Cholesterolemia
What the study found
Who was studied 14,320 Korean ancestry cases, 36,488 Korean ancestry controls.
The effect The reported allele is C; the catalogue records no effect size ; p = 3 × 10−16.
Where it sits Chromosome 7, band 7q21.11 — a missense change in CD36.
What ClinVar records
Classification
Conflicting classifications of pathogenicity for Platelet-type bleeding disorder 10, Inherited bleeding disorder, platelet-type; criteria provided, conflicting classifications (1 of 4 stars, 9 submitters), last evaluated 2026-01-05.
ClinVar record 13535 NM_001001548.3(CD36):c.268C>T (p.Pro90Ser)
What this is ClinVar's aggregate record for this position (as of its 2026-09-24 release), not a result about you. A classification describes the variant against the condition named, as laboratories submitted it. Whether a person carries this variant, and what that would mean for them, is a question for a clinical test and a genetic counsellor.
rs75326924 is a single position in the genome, in or near the CD36 gene. Published research associates it with hypo-hdl-cholesterolemia. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
On MyGeneLog this position is linked to Hypo-HDL-Cholesterolemia. The research behind each link, and its sources, are set out on that condition page.
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.
GWAS Catalog, International journal of molecular sciences 2022, PMID:36233190. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
Free to quote and reuse under CC BY 4.0. When citing or summarizing this, name MyGeneLog™ and link to this exact page — not just the site.
Hypo-HDL-cholesterolemia (rs75326924). MyGeneLog™. https://www.mygenelog.com/variants/rs75326924