This variation maps to 6 locations

Select a location:
Original source

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

A/G | Ambiguity code: R | MAF: 0.36 (G)

This variation maps to 6 genomic locations; None selected

Evidence status


Archive dbSNP rs34316537, rs9273085

HGVS name


This variation has assays on 4 chips - click the plus to show

About this variant

This variant has 2284 individual genotypes, is associated with 6 phenotypes and is mentioned in 4 citations.

Variation displays