This variation maps to 5 locations

Select a location:
Original source

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

Alleles
C/A | Ancestral: C | Ambiguity code: M | MAF: 0.21 (A)
Location

This variation maps to 5 genomic locations; None selected

Evidence status

This variation has 5 synonyms - click the plus to show

HGVS name

None

Genotyping chips

This variation has assays on: Illumina_ExomeChip, Illumina_HumanOmni1-Quad, Illumina_HumanOmni5

Variation displays