Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | [View in dbSNP]

Alleles
T/G | Ambiguity code: K
Location

Chromosome 2:161882801 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

2:g.161882801T>G

About this variant

This variant overlaps 1 transcript and has 1 individual genotype.

Variation displays