Original source

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

Alleles
T/G|Ancestral: T|Ambiguity code: K
Location

Chromosome 2:118847741 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

HGVS name

2:g.118847741T>G

About this variant

This variant overlaps 2 transcripts and 1 regulatory feature.

Variant displays