Original source

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

Alleles
A/G | Ancestral: A | Ambiguity code: R | MAF: 0.35 (G)
Location

Chromosome 12:52313826 (forward strand) | View in location tab

Most severe consequence
 
Downstream gene variant
Evidence status

HGVS name

12:g.52313826A>G

Genotyping chips

This variant has assays on: Illumina_Human660W-quad

About this variant

This variant overlaps 3 transcripts and has 2582 sample genotypes.

Variant displays