This variation maps to 2 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: 0.02 (C)
Location

This variation maps to 2 genomic locations; None selected

Evidence status

Synonyms

Archive dbSNP rs117133971, rs116478228

HGVS name

None

Genotyping chips

This variation has assays on: Illumina_HumanOmni2.5

Variation displays