This variation has been flagged

Variation maps to 2 genomic locations

Select a location:
Original source

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

Alleles
C/T | Ambiguity code: Y
Location

This variation maps to 2 genomic locations; None selected

HGVS name

None

Genotyping chips

This variation has assays on: Illumina_HumanOmni1-Quad, Illumina_1M-duo

Variation displays