Original source

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

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

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

Most severe consequence
Non coding transcript exon variant
Evidence status


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