Original source

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

Alleles
A/G | Ancestral: A | Ambiguity code: R
Location

Chromosome 2:232539110 (forward strand) | View in location tab

Most severe consequence
HGVS name

2:g.232539110A>G

About this variant

This variant overlaps 8 transcripts and has 1 individual genotype.

Variation displays