Variant (rsID / SNP)

rs8187832

rs8187832 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC15A1. Location: chromosome 13, position 99,340,771. The table records no clinical significance for this variant.

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Reference-table entries

SLC15A1Not classified

Variant type: synonymous_variant
Chromosome / position: 13:99340771
HGVS: NM_005073.4,c.1527C>T,p.Asn509Asn
Allele change: Synonymous_N509N

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.