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Variant (rsID / SNP)

rs11854484

SLC28A2

rs11854484 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC28A2. Location: chromosome 15, position 45,545,478. The table records no clinical significance for this variant.

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Reference-table entries

SLC28A2Not classified
Variant type
missense_variant
Chromosome / position
15:45545478
HGVS
NM_004212.4,c.65C>T,p.Pro22Leu
Allele change
Silent

Associated conditions / phenotypes

Hepatitis C

Public references

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