Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
G/A | Ambiguity code: R
Location

Chromosome 2:232538993 (forward strand) | View in location tab

Most severe consequence
HGVS name

2:g.232538993G>A

About this variant

This variant overlaps 7 transcripts and has 267 individual genotypes.

Variation displays