Variant (rsID / SNP)
rs12529
rs12529 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to AKR1C3. Location: chromosome 10, position 5,136,651. The table records no clinical significance for this variant.
Reference-table entries
AKR1C3Not classified
- Variant type
- missense_variant
- Chromosome / position
- 10:5136651
- HGVS
- NM_001253909.2,c.15C>G,p.His5Gln
- Allele change
- Silent
Associated conditions / phenotypes
Prostate Cancer|Polycystic Ovary Syndrome|Bladder Cancer|Alcohol Dependence|Lung Cancer
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.