Original source

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

Alleles
A/G | Ancestral: G | Ambiguity code: R | MAF: 0.12 (G)
Location

Chromosome 6:12715289 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

6:g.12715289A>G

Genotyping chips

This variation has assays on: Illumina_Cardio-Metabo_Chip

Variation displays