Original source

Variants (including SNPs and indels) imported from dbSNP (release 143)|View in dbSNP

Alleles
T/G|Ambiguity code: K
Location

Chromosome 2:26997417 (forward strand)|View in location tab

Most severe consequence
 
Missense variant
Evidence status

HGVS names

This variant has 3 HGVS names - Show

About this variant

This variant overlaps 1 transcript and has 192 sample genotypes.

Variant displays