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Variant (rsID / SNP)

rs2290272

SLC28A1

rs2290272 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC28A1. Location: chromosome 15, position 85,447,431. The table records no clinical significance for this variant.

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Reference-table entries

SLC28A1Not classified
Variant type
missense_variant
Chromosome / position
15:85447431
HGVS
NM_001287762.2,c.565G>A,p.Val189Ile
Allele change
Missense_V189I

Associated conditions / phenotypes

Hepatitis B

Public references

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