Original source

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

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

Chromosome 22:19150145 (forward strand) | View in location tab

Most severe consequence
Missense variant
Evidence status


Uniprot VAR_008549

HGVS names

This variant has 3 HGVS names - Show

About this variant

This variant overlaps 1 transcript and has 2504 sample genotypes.

Variant displays