Variant (rsID / SNP)
rs2234636
rs2234636 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC39A2. Location: chromosome 14, position 21,469,151. The table records no clinical significance for this variant.
Reference-table entries
SLC39A2Not classified
- Variant type
- missense_variant
- Chromosome / position
- 14:21469151
- HGVS
- NM_014579.4,c.343T>C,p.Phe115Leu
- Allele change
- Silent
Associated conditions / phenotypes
Bladder Cancer
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.