Original source

Variants (including SNPs and indels) imported from dbSNP (release 136)|View in dbSNP

Alleles
A/G|Ancestral: A|Ambiguity code: R
Location

Chromosome 4:83029642 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
HGVS name

4:g.83029642A>G

About this variant

This variant overlaps 2 transcripts.

Variant displays