rs662
NM_000446.7(PON1):c.575A>G (p.Gln192Arg)
- Coronary artery disease, susceptibility toRisk factor · germline
- Coronary artery spasm 2, susceptibility toRisk factor · germline
- PON1-related disorderBenign · germline
- Enzyme activity findingassociation · germline
- not providedBenign · ★★ · germline
gnomAD allele frequency 4.07e-1
rs662 is a genetic variant located in the PON1 gene. dbsnp · gene
In gnomAD, rs662 has an overall allele frequency of 40.7%. gnomad · frequency
In ClinVar, rs662 is classified as Risk factor for Coronary artery disease, susceptibility to (0 review stars, germline; last evaluated 2011-01-01). clinvar · classificationclinvar · review confidenceclinvar · originclinvar · assertion date
In ClinVar, rs662 is classified as Risk factor for Coronary artery spasm 2, susceptibility to (0 review stars, germline; last evaluated 2011-01-01). clinvar · classificationclinvar · review confidenceclinvar · originclinvar · assertion date
In ClinVar, rs662 is classified as Benign for PON1-related disorder (0 review stars, germline; last evaluated 2019-10-18). clinvar · classificationclinvar · review confidenceclinvar · originclinvar · assertion date
In ClinVar, rs662 is classified as association for Enzyme activity finding (0 review stars, germline; last evaluated 2015-05-18). clinvar · classificationclinvar · review confidenceclinvar · originclinvar · assertion date
In ClinVar, rs662 is classified as Benign for not provided (2 review stars, germline; last evaluated 2019-05-23). clinvar · classificationclinvar · review confidenceclinvar · originclinvar · assertion date
retrieved 2026-08-03 · facts c1ad6388cf3f651d · 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.