Original source

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

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

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

Most severe consequence
 
Missense variant
Evidence status

Synonyms

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