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
A/C | Ancestral: A | Ambiguity code: M | MAF: 0.19 (C)
Location

This variation maps to 2 genomic locations; None selected

Evidence status

HGVS name

None

Genotyping chips

This variation has assays on: Illumina_ImmunoChip

Variation displays