This variation has been flagged

Variation has more than 3 different alleles

Select a location:
Original source

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

Alleles
A/C/G/T | Ambiguity code: N | MAF: 0.10 (C)
Location

This variation maps to 6 genomic locations; None selected

Evidence status

Synonyms
HGVS name

None

Genotyping chips

This variation has assays on: Illumina_1M-duo, Illumina_HumanOmni1-Quad, Illumina_HumanOmni5

Variation displays