Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.02 (A)
Location

Chromosome 12:52468081 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

12:g.52468081G>A

Genotyping chips

This variation has assays on: Illumina_HumanOmni1-Quad

About this variant

This variant overlaps 3 transcripts and has 2773 individual genotypes.

Variation displays