This variation maps to 5 locations

Select a location:
Original source

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

Alleles
C/G | Ambiguity code: S | MAF: 0.40 (G)
Location

This variation maps to 5 genomic locations; None selected

Evidence status

This variation has 7 synonyms - click the plus to show

HGVS name

None

Genotyping chips

This variation has assays on: Illumina_ExomeChip, Illumina_HumanOmni1-Quad

Variation displays