Original source

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

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

Chromosome 12:56078510 (forward strand) | View in location tab

Co-located

with dbSNP rs567937960 (G/-)

Most severe consequence
 
Upstream gene variant
HGVS name

12:g.56078510G>A

About this variant

This variant overlaps 10 transcripts.

Variant displays