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
G/A | Ambiguity code: R | MAF: 0.24 (G)
Location

This variation maps to 2 genomic locations; None selected

Evidence status

Synonyms

Archive dbSNP rs56479386, rs60477402

HGVS name

None

Genotyping chips

This variation has assays on: Affy GeneChip 500K, Illumina_ImmunoChip, Affy GenomeWideSNP_6.0

Variation displays