Variant (rsID / SNP)
rs2293616
rs2293616 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC15A2. Location: chromosome 3, position 121,641,693. The table records no clinical significance for this variant.
Reference-table entries
SLC15A2Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 3:121641693
- HGVS
- NM_021082.4,c.852G>A,p.Ala284Ala
- Allele change
- Synonymous_A284A
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.