Variant (rsID / SNP)
rs2180314
rs2180314 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GSTA2. Location: chromosome 6, position 52,617,731. The table records no clinical significance for this variant.
Reference-table entries
GSTA2Not classified
- Variant type
- missense_variant
- Chromosome / position
- 6:52617731
- HGVS
- NM_000846.5,c.335G>C,p.Ser112Thr
- Allele change
- Missense_S112T
Associated conditions / phenotypes
Breast Cancer
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.