Variant (rsID / SNP)
rs8187838
rs8187838 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC15A1. Location: chromosome 13, position 99,356,607. The table records no clinical significance for this variant.
Reference-table entries
SLC15A1Not classified
- Variant type
- missense_variant
- Chromosome / position
- 13:99356607
- HGVS
- NM_005073.4,c.1352C>A,p.Thr451Asn
- Allele change
- Missense_T451N
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.