This variant maps to 2 locations

Select a location:
Original source

Variants (including SNPs and indels) imported from dbSNP (release 144) | View in dbSNP

A/G | Ancestral: A | Ambiguity code: R | MAF: 0.40 (G)

This variant maps to 2 genomic locations; None selected

Evidence status

Clinical significance


This variant has 5 synonyms - Show

HGVS name


Genotyping chips

This variant has assays on 12 chips - Show

About this variant

This variant has 4071 sample genotypes, is associated with 13 phenotypes and is mentioned in 157 citations.

Variant displays