Original source

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

Alleles
G/A/T|Ancestral: G|Ambiguity code: D|MAF: < 0.01 (A)
Location

Chromosome 3:49899193 (forward strand)|View in location tab

Most severe consequence
 
Stop gained
Evidence status

Synonyms

Uniprot VAR_029238

HGVS names

This variant has 28 HGVS names - Show

Genotyping chips

This variant has assays on 4 chips - Show

About this variant

Variant displays