rs59421388
NM_000106.6(CYP2D6):c.1012G>A (p.Val338Met)
- not providedLikely benign · ★★ · germline
gnomAD allele frequency 2.59e-2
rs59421388 is a genetic variant located in the CYP2D6 gene. dbsnp · gene
In gnomAD, rs59421388 has an overall allele frequency of 2.6%. gnomad · frequency
In ClinVar, rs59421388 is classified as Likely benign for not provided (2 review stars, germline; last evaluated 2018-08-06). clinvar · classificationclinvar · review confidenceclinvar · originclinvar · assertion date
retrieved 2026-08-03 · facts eb3853eab30e5dca · 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.