Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

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

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

Most severe consequence
 
Upstream gene variant
Evidence status

HGVS name

2:g.232539110A>G

About this variant

This variant overlaps 7 transcripts, 1 regulatory feature and has 1 sample genotype.

Variant displays