Original source

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

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

Chromosome 16:31191077 (forward strand) | View in location tab

Most severe consequence
Missense variant
Evidence status

HGVS names

This variant has 15 HGVS names - Show

About this variant

This variant overlaps 12 transcripts and has 2 sample genotypes.

Variant displays