Variant (rsID / SNP)
rs624249
rs624249 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC22A2. Location: chromosome 6, position 160,679,400. The table records no clinical significance for this variant.
Reference-table entries
SLC22A2Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 6:160679400
- HGVS
- NM_003058.4,c.390G>T,p.Thr130Thr
- Allele change
- Synonymous_T130T
Associated conditions / phenotypes
Rheumatoid Arthritis|Arthritis
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.