rs1045642
NM_001348946.2(ABCB1):c.3435T>C (p.Ile1145=)
- Tramadol responseDrug response · somatic
- ABCB1-related disorderLikely benign · germline
- MDR1 POLYMORPHISMBenign · germline
- not providedBenign · ★★ · germline
gnomAD allele frequency 5.60e-1
rs1045642 is a genetic variant located in the ABCB1 gene. dbsnp · gene
In gnomAD, rs1045642 has an overall allele frequency of 56.0%. gnomad · frequency
In ClinVar, rs1045642 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, rs1045642 is classified as Likely benign for ABCB1-related disorder (0 review stars, germline; last evaluated 2021-07-21). clinvar · classificationclinvar · review confidenceclinvar · originclinvar · assertion date
In ClinVar, rs1045642 is classified as Benign for MDR1 POLYMORPHISM (0 review stars, germline; last evaluated 2007-01-26). clinvar · classificationclinvar · review confidenceclinvar · originclinvar · assertion date
In ClinVar, rs1045642 is classified as Benign for not provided (2 review stars, germline; last evaluated 2018-03-13). clinvar · classificationclinvar · review confidenceclinvar · originclinvar · assertion date
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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.