This variant maps to 8 locations

Select a location:
Original source

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

Alleles
A/G/T|Ambiguity code: D|MAF: 0.38 (G)
Location

This variant maps to 8 genomic locations; None selected

Evidence status

HGVS name

None

Genotyping chips

This variant has assays on: Illumina_HumanOmni5

About this variant

This variant has 2510 sample genotypes.

Variant displays