Original source

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

Alleles
G/C|Ancestral: G|Ambiguity code: S|MAF: 0.12 (C)
Location

Chromosome 22:50581640 (forward strand)|View in location tab

Most severe consequence
 
Non coding transcript exon variant
Evidence status

Synonyms

Archive dbSNP rs5770787

HGVS names

This variant has 13 HGVS names - Show

About this variant

This variant overlaps 26 transcripts, has 2773 sample genotypes and is mentioned in 1 citation.

Variant displays