rs3892097
CYP2D6*4
- Tamoxifen responseDrug response · ★ · germline
- Deutetrabenazine responseDrug response · ★ · germline
- Tramadol responseDrug response · somatic
- Debrisoquine, poor metabolism ofDrug response · germline
- not specifiedLikely benign · ★ · germline
- not providedother · ★ · germline
gnomAD allele frequency 1.37e-1
rs3892097 is a genetic variant located in the CYP2D6 gene. dbsnp · gene
In gnomAD, rs3892097 has an overall allele frequency of 13.7%. gnomad · frequency
In ClinVar, rs3892097 is classified as Drug response for Tamoxifen response (1 review star, germline; last evaluated 2019-05-01). clinvar · classificationclinvar · review confidenceclinvar · originclinvar · assertion date
In ClinVar, rs3892097 is classified as Drug response for Deutetrabenazine response (1 review star, germline; last evaluated 2019-05-01). clinvar · classificationclinvar · review confidenceclinvar · originclinvar · assertion date
In ClinVar, rs3892097 is classified as Drug response for Tramadol response (0 review stars, somatic; last evaluated 2018-04-28). clinvar · classificationclinvar · review confidenceclinvar · originclinvar · assertion date
In ClinVar, rs3892097 is classified as Drug response for Debrisoquine, poor metabolism of (0 review stars, germline; last evaluated 2015-05-18). clinvar · classificationclinvar · review confidenceclinvar · originclinvar · assertion date
In ClinVar, rs3892097 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, rs3892097 is classified as other for not provided (1 review star, germline; last evaluated 2018-08-06). clinvar · classificationclinvar · review confidenceclinvar · originclinvar · assertion date
retrieved 2026-08-03 · facts c194e7ed6b05160f · 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.