Original source

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

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

Chromosome 9:122204712 (forward strand) | View in location tab

Most severe consequence
Missense variant
Evidence status


Archive dbSNP rs3206376

HGVS names

This variant has 13 HGVS names - Show

About this variant

This variant overlaps 11 transcripts, 1 regulatory feature and has 1 sample genotype.

Variant displays