Variant (rsID / SNP)
rs12659
rs12659 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC19A1. Location: chromosome 21, position 46,951,556. The table records no clinical significance for this variant.
Reference-table entries
SLC19A1Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 21:46951556
- HGVS
- NM_001352512.2,c.696T>C,p.Pro232Pro
- Allele change
- Synonymous_P114P
Associated conditions / phenotypes
Synonymous_P192P
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.