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 3:171027031 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
HGVS name

3:g.171027031A>G

About this variant

This variant overlaps 3 transcripts.

Variant displays