Original source

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

G/A | Ambiguity code: R | MAF: 0.12 (A)

Chromosome 6:32642972 (forward strand) | View in location tab

Most severe consequence
Missense variant
Evidence status

HGVS names

This variant has 8 HGVS names - Show

About this variant

This variant overlaps 6 transcripts and has 2506 sample genotypes.

Variant displays