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Variant (rsID / SNP)

rs12422149

SLCO2B1

rs12422149 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLCO2B1. Location: chromosome 11, position 74,883,577. The table records no clinical significance for this variant.

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Reference-table entries

SLCO2B1Not classified
Variant type
missense_variant
Chromosome / position
11:74883577
HGVS
NM_007256.5,c.935G>A,p.Arg312Gln
Allele change
Missense_R312Q

Associated conditions / phenotypes

Prostate Cancer|Atherosclerosis Susceptibility|Myopathy

Public references

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