rs1801282
NM_138711.6(PPARG):c.-8-28078C>G
- INSULIN RESISTANCE, DIGENICLikely benign · ★ · germline
- PPARG-related familial partial lipodystrophyLikely benign · ★ · germline
- ObesityLikely benign · ★ · germline
- not providedLikely benign · ★★ · germline
- not specifiedLikely benign · germline
gnomAD allele frequency 1.00e-1
rs1801282 is a genetic variant located in the PPARG gene. dbsnp · gene
In gnomAD, rs1801282 has an overall allele frequency of 10.0%. gnomad · frequency
In ClinVar, rs1801282 is classified as Likely benign for INSULIN RESISTANCE, DIGENIC (1 review star, germline; last evaluated 2017-04-27). clinvar · classificationclinvar · review confidenceclinvar · originclinvar · assertion date
In ClinVar, rs1801282 is classified as Likely benign for PPARG-related familial partial lipodystrophy (1 review star, germline; last evaluated 2017-04-27). clinvar · classificationclinvar · review confidenceclinvar · originclinvar · assertion date
In ClinVar, rs1801282 is classified as Likely benign for Obesity (1 review star, germline; last evaluated 2017-04-27). clinvar · classificationclinvar · review confidenceclinvar · originclinvar · assertion date
In ClinVar, rs1801282 is classified as Likely benign for not provided (2 review stars, germline; last evaluated 2025-02-02). clinvar · classificationclinvar · review confidenceclinvar · originclinvar · assertion date
In ClinVar, rs1801282 is classified as Likely benign for not specified (0 review stars, germline). clinvar · classificationclinvar · review confidenceclinvar · origin
retrieved 2026-08-03 · facts ad9070977b6354e7 · 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.