Original source

Variants (including SNPs and indels) imported from dbSNP (release 140) | [View in dbSNP]

Alleles
T/G | Ambiguity code: K
Location

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

Most severe consequence
Evidence status

This variation has 3 HGVS names - click the plus to show

About this variant

This variant overlaps 1 transcript and has 184 individual genotypes.

Variation displays