This variant maps to 2 locations

Select a location:
Original source

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

Alleles
T/A/C | Ancestral: T | Ambiguity code: H
Location

This variant maps to 2 genomic locations; None selected

HGVS name

None

Genotyping chips

This variant has assays on: Illumina_Human1M-duo, Illumina_HumanOmni5

Variant displays