This variation maps to 2 locations

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Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

T/C | Ancestral: C | Ambiguity code: Y | MAF: 0.35 (C)

This variation maps to 2 genomic locations; None selected

Evidence status


Archive dbSNP rs34912150, rs59821819

HGVS name


This variation has assays on 13 chips - click the plus to show

About this variant

This variant has 4279 individual genotypes, is associated with 3 phenotypes and is mentioned in 17 citations.

Variation displays