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
G/C | Ancestral: G | Ambiguity code: S | MAF: 0.14 (C)
Location

This variation maps to 5 genomic locations; None selected

Evidence status

Clinical significance

This variation has 7 synonyms - click the plus to show

HGVS name

None

Genotyping chips

This variation has assays on: HumanCoreExome-12, Illumina_HumanOmni5

Variation displays