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Variant (rsID / SNP)

rs1517618

SLCO3A1

rs1517618 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLCO3A1. Location: chromosome 15, position 92,647,645. The table records no clinical significance for this variant.

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Reference-table entries

SLCO3A1Not classified
Variant type
missense_variant
Chromosome / position
15:92647645
HGVS
NM_013272.4,c.882G>C,p.Glu294Asp
Allele change
Missense_E294D

Public references

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