Original source

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

Alleles
A/G|Ancestral: G|Ambiguity code: R|MAF: 0.16 (G)
Location

Chromosome 22:50584911 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs57456372, rs7284813

HGVS names

This variant has 3 HGVS names - Show

About this variant

Variant displays