Original source

Variants (including SNPs and indels) imported from dbSNP (release 139) | [View in dbSNP]

A/T | Ambiguity code: W

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

Most severe consequence

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

About this variant

This variant overlaps 1 transcript and has 1 individual genotype.

Variation displays