This variation maps to 6 locations

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Original source

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

A/G | Ancestral: A | Ambiguity code: R | MAF: 0.04 (G)

This variation maps to 6 genomic locations; None selected

Evidence status


Archive dbSNP rs114823772, rs59522889

HGVS name


This variation has assays on 11 chips - click the plus to show

About this variant

This variant has 1859 individual genotypes, is associated with 6 phenotypes and is mentioned in 2 citations.

Variation displays