This variant maps to 2 locations

Select a location:
Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
C/G/T|Ancestral: C|Ambiguity code: B|MAF: 0.04 (T)
Location

This variant maps to 2 genomic locations; None selected

Evidence status

HGVS name

None

Genotyping chips

This variant has assays on: Illumina_Cardio-Metabo_Chip, Illumina_HumanOmni5

About this variant

This variant has 2552 sample genotypes.

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