Original source

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

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

Chromosome 8:48923234 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
HGVS name

8:g.48923234G>A

About this variant

This variant overlaps 2 transcripts and 1 regulatory feature.

Variant displays