rs1695
NM_000852.4(GSTP1):c.313A>G (p.Ile105Val)
- Abnormality of immune system physiologyBenign · unknown
- GLUTATHIONE S-TRANSFERASE PI POLYMORPHISM, TYPE BBenign · germline
- GLUTATHIONE S-TRANSFERASE PI POLYMORPHISM, TYPE CBenign · germline
- not providedBenign · ★★ · germline
gnomAD allele frequency 3.53e-1
rs1695 is a genetic variant located in the GSTP1 gene. dbsnp · gene
In gnomAD, rs1695 has an overall allele frequency of 35.3%. gnomad · frequency
In ClinVar, rs1695 is classified as Benign for Abnormality of immune system physiology (0 review stars; last evaluated 2021-09-06). clinvar · classificationclinvar · review confidenceclinvar · assertion date
In ClinVar, rs1695 is classified as Benign for GLUTATHIONE S-TRANSFERASE PI POLYMORPHISM, TYPE B (0 review stars, germline; last evaluated 1997-04-11). clinvar · classificationclinvar · review confidenceclinvar · originclinvar · assertion date
In ClinVar, rs1695 is classified as Benign for GLUTATHIONE S-TRANSFERASE PI POLYMORPHISM, TYPE C (0 review stars, germline; last evaluated 1997-04-11). clinvar · classificationclinvar · review confidenceclinvar · originclinvar · assertion date
In ClinVar, rs1695 is classified as Benign for not provided (2 review stars, germline; last evaluated 2021-06-09). 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.