Variant (rsID / SNP)
rs1131596
rs1131596 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC19A1. Location: chromosome 21, position 46,957,916. The table records no clinical significance for this variant.
Reference-table entries
SLC19A1Not classified
- Variant type
- 5_prime_UTR_variant
- Chromosome / position
- 21:46957916
- HGVS
- NM_001352512.2,c.-43C>T
- Allele change
- Silent
Associated conditions / phenotypes
Acute Leukemia|Leukemia|Rheumatoid Arthritis|Methotrexate Toxicity
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.