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Variant (rsID / SNP)

rs1143671

SLC15A2

rs1143671 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC15A2. Location: chromosome 3, position 121,647,286. The table records no clinical significance for this variant.

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Reference-table entries

SLC15A2Not classified
Variant type
missense_variant
Chromosome / position
3:121647286
HGVS
NM_021082.4,c.1225C>T,p.Pro409Ser
Allele change
Missense_P409S

Public references

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