Original source

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

G/A/C | Ancestral: G | Ambiguity code: V

Chromosome 3:49121244 (forward strand) | View in location tab

Most severe consequence
Missense variant
Evidence status

HGVS names

This variant has 14 HGVS names - Show

Genotyping chips

This variant has assays on 4 chips - Show

About this variant

This variant overlaps 60 transcripts and has 2 sample genotypes.

Variant displays