Original source

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

Alleles
G/A|Ancestral: G|Ambiguity code: R|MAF: 0.30 (A)
Location

Chromosome 22:50630132 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

Synonyms

Archive dbSNP rs61123803

HGVS name

22:g.50630132G>A

Genotyping chips

This variant has assays on 9 chips - Show

About this variant

This variant overlaps 7 transcripts and has 3691 sample genotypes.

Variant displays