This variation has been flagged

None of the variant alleles match the reference allele

Select a location:
Original source

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

Alleles
C/A | Ancestral: C | Ambiguity code: M | MAF: 0.04 (A)
Location

This variation maps to 2 genomic locations; None selected

Evidence status

Synonyms

Archive dbSNP rs117321595

HGVS name

None

Genotyping chips

This variation has assays on: Illumina_ImmunoChip, Illumina_HumanOmni2.5, Illumina_HumanOmni5

Variation displays