Original source

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

Alleles
C/G|Ancestral: C|Ambiguity code: S|MAF: 0.37 (G)
Location

Chromosome 12:52314189 (forward strand)|View in location tab

Most severe consequence
 
Downstream gene variant
Evidence status

HGVS name

12:g.52314189C>G

About this variant

This variant overlaps 1 transcript and has 2510 sample genotypes.

Variant displays