Original source

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

Alleles
A/T|Ambiguity code: W
Location

Chromosome 2:94992641 (forward strand)|View in location tab

Most severe consequence
 
Stop gained
HGVS names

This variant has 3 HGVS names - Show

About this variant

This variant overlaps 1 transcript and has 1 sample genotype.

Variant displays