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/G | Ancestral: G | Ambiguity code: S | MAF: 0.21 (C)
Location

This variation maps to 2 genomic locations; None selected

Evidence status

Synonyms

Archive dbSNP rs36224309

HGVS name

None

Genotyping chips

This variation has assays on: Affy GenomeWideSNP_6.0

Variation displays