Original source

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

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

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

Most severe consequence
HGVS name

3:g.58427420T>A

About this variant

This variant overlaps 20 transcripts.

Variation displays