Original source

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

Alleles
A/G | Ambiguity code: R | MAF: 0.29 (A)
Location

Chromosome 12:52314267 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

12:g.52314267A>G

About this variant

This variant overlaps 1 transcript and has 2507 individual genotypes.

Variation displays