Original source

Variants (including SNPs and indels) imported from dbSNP (release 136)|View in dbSNP

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

Chromosome 13:49751323 (forward strand)|View in location tab

Most severe consequence
Missense variant
HGVS names

This variant has 3 HGVS names - Show

About this variant

This variant overlaps 1 transcript and has 5 sample genotypes.

Variant displays