Original source

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

Alleles
A/C|Ancestral: A|Ambiguity code: M|MAF: 0.02 (C)
Location

Chromosome 12:56078502 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

HGVS name

12:g.56078502A>C

About this variant

This variant overlaps 10 transcripts and has 2504 sample genotypes.

Variant displays