Original source

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

T/A | Ancestral: T | Ambiguity code: W | MAF: 0.30 (A)

Chromosome 22:29280706 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs5763127

HGVS names

This variant has 16 HGVS names - Show

About this variant

This variant overlaps 16 transcripts and has 2506 sample genotypes.

Variant displays