Original source

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