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Variant (rsID / SNP)

rs2257212

SLC15A2

rs2257212 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC15A2. Location: chromosome 3, position 121,643,804. The table records no clinical significance for this variant.

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Reference-table entries

SLC15A2Not classified
Variant type
missense_variant
Chromosome / position
3:121643804
HGVS
NM_021082.4,c.1048C>T,p.Leu350Phe
Allele change
Missense_L350F

Associated conditions / phenotypes

Hepatocellular Carcinoma

Public references

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