This variant has been flagged

None of the variant alleles match the reference allele

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Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
A/C|Ancestral: A|Ambiguity code: M|MAF: 0.21 (C)
Location

This variant maps to 8 genomic locations; None selected

Evidence status

HGVS name

None

Genotyping chips

This variant has assays on: HumanCoreExome-12, Illumina_HumanOmni1-Quad, Illumina_ExomeChip

About this variant

This variant has 2776 sample genotypes, is associated with 8 phenotypes and is mentioned in 3 citations.

Variant displays