rs1799853
CYP2C9*2
- Flurbiprofen responseDrug response · ★ · germline
- Lesinurad responseDrug response · ★ · germline
- Piroxicam responseDrug response · ★ · germline
- Phenytoin responseDrug response · germline
- Warfarin responseDrug response · germline
- not specifiedLikely benign · ★ · germline
- not providedother · ★ · germline
gnomAD allele frequency 8.25e-2
rs1799853 is a genetic variant located in the CYP2C9 gene. dbsnp · gene
In gnomAD, rs1799853 has an overall allele frequency of 8.2%. gnomad · frequency
In ClinVar, rs1799853 is classified as Drug response for Flurbiprofen response (1 review star, germline; last evaluated 2019-02-11). clinvar · classificationclinvar · review confidenceclinvar · originclinvar · assertion date
In ClinVar, rs1799853 is classified as Drug response for Lesinurad response (1 review star, germline; last evaluated 2019-02-11). clinvar · classificationclinvar · review confidenceclinvar · originclinvar · assertion date
In ClinVar, rs1799853 is classified as Drug response for Piroxicam response (1 review star, germline; last evaluated 2019-02-11). clinvar · classificationclinvar · review confidenceclinvar · originclinvar · assertion date
In ClinVar, rs1799853 is classified as Drug response for Phenytoin response (0 review stars, germline; last evaluated 2020-09-24). clinvar · classificationclinvar · review confidenceclinvar · originclinvar · assertion date
In ClinVar, rs1799853 is classified as Drug response for Warfarin response (0 review stars, germline; last evaluated 2018-08-09). clinvar · classificationclinvar · review confidenceclinvar · originclinvar · assertion date
In ClinVar, rs1799853 is classified as Likely benign for not specified (1 review star, germline; last evaluated 2018-03-09). clinvar · classificationclinvar · review confidenceclinvar · originclinvar · assertion date
In ClinVar, rs1799853 is classified as other for not provided (1 review star, germline; last evaluated 2015-07-09). clinvar · classificationclinvar · review confidenceclinvar · originclinvar · assertion date
retrieved 2026-08-03 · facts 397eae09edb2826a · 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.