This variant 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 (release 144)|View in dbSNP

Alleles
C/G|Ambiguity code: S|MAF: 0.11 (G)
Location

This variant maps to 6 genomic locations; None selected

Evidence status

Synonyms

This variant has 8 synonyms - Show

HGVS name

None

Genotyping chips

This variant has assays on: Illumina_Human1M-duo

About this variant

This variant has 2505 sample genotypes.

Variant displays