Variant (rsID / SNP)
rs4925
rs4925 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GSTO1. Location: chromosome 10, position 106,022,789. The table records no clinical significance for this variant.
Reference-table entries
- Variant type
- missense_variant
- Chromosome / position
- 10:106022789
- HGVS
- NM_004832.3,c.419C>A,p.Ala140Asp
- Allele change
- Missense_A112D
Associated conditions / phenotypes
Renal Cell Carcinoma, Nonpapillary|Alzheimer Disease|Bladder Cancer|Autosomal Dominant Cerebellar Ataxia|Ataxia and Polyneuropathy, Adult-Onset|Parkinson Disease, Late-Onset|Spinocerebellar Ataxia 2|Transitional Cell Carcinoma|Mild Cognitive Impairment|B-Lymphoblastic Leukemia/lymphoma|Leukemia|Polycystic Ovary Syndrome|Huntington Disease|Breast Cancer|Leukemia, Acute Lymphoblastic|End Stage Renal Disease|Cataract
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.