This variation maps to 6 locations

Select a location:
Original source

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

Alleles
C/G/T | Ancestral: C | Ambiguity code: B
Location

This variation maps to 6 genomic locations; None selected

Evidence status

Synonyms
HGVS name

None

Genotyping chips

This variation has assays on: Illumina_HumanOmni1-Quad

Variation displays