Original source

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

Alleles
A/C | Ancestral: A | Ambiguity code: M | MAF: 0.21 (A)
Location

Chromosome 12:52796606 (forward strand) | View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

Synonyms

Archive dbSNP rs61599856, rs12818335

HGVS name

12:g.52796606A>C

About this variant

This variant overlaps 1 transcript and has 2513 sample genotypes.

Variant displays