rs1695
rs1695 · SaudiVarKB evidence summary derived from retained literature mentions.
4Variant mentions
4Publications
3Associated gene records
2Associated phenotype records
Associated gene records
Co-mentioned in the same publicationsAssociated phenotype records
Co-mentioned in the same publications| Phenotype | Identifier / context | Articles | Mentions |
|---|---|---|---|
| hearing loss | HP:0000365 | 1 | 1 |
| breast cancer | — | 1 | 1 |
Associated population records
Co-mentioned in the same publications| Population | Identifier / context | Articles | Mentions |
|---|---|---|---|
| Population record | Cohort 200 | 1 | 1 |
| Population record | Cohort 64 | 1 | 1 |
Supporting publications
4 records- 2026Molecular dynamics investigation of single nucleotide polymorphism-driven variations in GSTP1 phosphorylation and substrate interaction.Journal of biomolecular structure & dynamics1 mentions
- 2024Exposure to heavy metals, antioxidant status, and the interaction of single nucleotide polymorphisms in the genes CAT rs7943316, GSTP1 rs1695, as well as GSTM1 and GSTT1 genes, among workers in occupational settings.Environmental toxicology and pharmacology1 mentions
- 2022Platinum-induced ototoxicity in pediatric cancer survivors: GSTP1 c.313A>G variant association.Medicine1 mentions
- 2021Association of GSTP1 p.Ile105Val (rs1695, c.313A > G) Variant with the Risk of Breast Carcinoma among Egyptian Women.Biochemical genetics1 mentions