Original source

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

Alleles
T/A|Ancestral: A|Ambiguity code: W
Location

Chromosome 3:58427420 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

HGVS name

3:g.58427420T>A

About this variant

This variant overlaps 20 transcripts.

Variant displays