Original source

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

Alleles
A/C | Ancestral: A | Ambiguity code: M
Location

Chromosome 2:232539308 (forward strand) | View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

HGVS name

2:g.232539308A>C

About this variant

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

Variant displays