rs5882
NM_000078.3(CETP):c.1264G>A (p.Val422Ile)
- Coronary artery disorderBenign · ★ · germline
- Hyperalphalipoproteinemia 1 (HALP1)Benign · ★ · germline
- High density lipoprotein cholesterol level quantitative trait locus 10association · germline
- not providedBenign · ★★ · germline
- not specifiedBenign · germline
gnomAD allele frequency 5.94e-1
rs5882 is a genetic variant located in the CETP gene. dbsnp · gene
In gnomAD, rs5882 has an overall allele frequency of 59.4%. gnomad · frequency
In ClinVar, rs5882 is classified as Benign for Coronary artery disorder (1 review star, germline; last evaluated 2022-05-12). clinvar · classificationclinvar · review confidenceclinvar · originclinvar · assertion date
In ClinVar, rs5882 is classified as Benign for Hyperalphalipoproteinemia 1 (HALP1) (1 review star, germline; last evaluated 2017-04-27). clinvar · classificationclinvar · review confidenceclinvar · originclinvar · assertion date
In ClinVar, rs5882 is classified as association for High density lipoprotein cholesterol level quantitative trait locus 10 (0 review stars, germline; last evaluated 2010-01-13). clinvar · classificationclinvar · review confidenceclinvar · originclinvar · assertion date
In ClinVar, rs5882 is classified as Benign for not provided (2 review stars, germline; last evaluated 2025-02-03). clinvar · classificationclinvar · review confidenceclinvar · originclinvar · assertion date
In ClinVar, rs5882 is classified as Benign for not specified (0 review stars, germline). clinvar · classificationclinvar · review confidenceclinvar · origin
retrieved 2026-08-03 · facts 39acfc48c0373851 · meta/llama-3.1-8b-instruct · prompt 4.0.1 · schema 3.0.0
Educational information only — not medical advice, a diagnosis, or a clinical interpretation. A variant's significance can be uncertain, conflicting, or dependent on your full clinical and family context. Consult a qualified genetics professional or genetic counselor before drawing any conclusion.