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
A/C|Ancestral: A|Ambiguity code: M|MAF: 0.06 (C)
Location

This variant maps to 10 genomic locations; None selected

Evidence status

HGVS name

None

Genotyping chips

This variant has assays on: Illumina_Human1M-duo, Illumina_HumanHap650Y, Illumina_HumanOmni5

About this variant

This variant has 3504 sample genotypes.

Variant displays