This variation maps to 2 locations

Select a location:
Original source

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

Alleles
A/G | Ancestral: A | Ambiguity code: R | MAF: 0.01 (G)
Location

This variation maps to 2 genomic locations; None selected

Evidence status

HGVS name

None

Genotyping chips

This variation has assays on: Illumina_Cardio-Metabo_Chip

About this variant

This variant has 2504 individual genotypes.

Variation displays