rs2032582
NM_001348946.2(ABCB1):c.2677T>G (p.Ser893Ala)
- Inflammatory bowel disease 13 (IBD13)Risk factor · germline
- Tramadol responseDrug response · somatic
- ABCB1-related disorderLikely benign · germline
- not providedBenign · ★★ · germline
- not specifiedBenign · ★ · germline
gnomAD allele frequency 6.37e-1
rs2032582 is a genetic variant located in the ABCB1 gene. dbsnp · gene
In gnomAD, rs2032582 has an overall allele frequency of 63.7%. gnomad · frequency
In ClinVar, rs2032582 is classified as Risk factor for Inflammatory bowel disease 13 (IBD13) (0 review stars, germline; last evaluated 2003-12-01). clinvar · classificationclinvar · review confidenceclinvar · originclinvar · assertion date
In ClinVar, rs2032582 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, rs2032582 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, rs2032582 is classified as Benign for not provided (2 review stars, germline; last evaluated 2018-03-13). clinvar · classificationclinvar · review confidenceclinvar · originclinvar · assertion date
In ClinVar, rs2032582 is classified as Benign for not specified (1 review star, germline; last evaluated 2014-01-27). 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.