Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.04 (A)
Location

Chromosome 6:12715537 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

6:g.12715537G>A

Genotyping chips

This variation has assays on: Illumina_Cardio-Metabo_Chip, Illumina_HumanOmni2.5, Illumina_HumanOmni5

Variation displays