Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | View in dbSNP

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

Chromosome 6:12715305 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

6:g.12715305G>A

Genotyping chips

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

Variation displays