This variation maps to 8 locations

Select a location:
Original source

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

Alleles
A/C/T | Ancestral: A | Ambiguity code: H | MAF: 0.35 (C)
Location

This variation maps to 8 genomic locations; None selected

Evidence status

Synonyms
HGVS name

None

Genotyping chips

This variation has assays on: Illumina_1M-duo, Illumina_HumanOmni1-Quad, Illumina_HumanOmni2.5

Variation displays