This variation maps to 8 locations

Select a location:
Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | View in dbSNP

Alleles
A/G/T | Ambiguity code: D | MAF: 0.36 (G)
Location

This variation maps to 8 genomic locations; None selected

Evidence status

HGVS name

None

Genotyping chips

This variation has assays on: Illumina_HumanOmni5

Variation displays