This variation maps to 7 locations

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Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.05 (T)

This variation maps to 7 genomic locations; None selected

Evidence status


Archive dbSNP rs116138574, rs117316167

HGVS name


This variation has assays on 7 chips - click the plus to show

About this variant

This variant has 2282 individual genotypes, is associated with 7 phenotypes and is mentioned in 3 citations.

Variation displays