Original source

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

G/A|Ancestral: G|Ambiguity code: R

Chromosome 11:44292029 (forward strand)|View in location tab

Co-located variant

dbSNP rs528462442 (G/-)

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs454637

HGVS names

This variant has 2 HGVS names - Show

About this variant

This variant overlaps 1 transcript and has 2 sample genotypes.

Variant displays