This variation maps to 2 locations

Select a location:
Original source

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

Alleles
A/T | Ancestral: T | Ambiguity code: W | MAF: 0.30 (A)
Location

This variation maps to 2 genomic locations; None selected

Evidence status

HGVS name

None

Genotyping chips

This variation has assays on: Affy GenomeWideSNP_6.0, Illumina_CytoSNP12v1

Variation displays