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

G/C|Ancestral: G|Ambiguity code: S|MAF: 0.20 (C)

This variant maps to 5 genomic locations; None selected

Evidence status

Clinical significance


This variant has 7 synonyms - Show

HGVS name


Genotyping chips

This variant has assays on: HumanCoreExome-12, Illumina_HumanOmni5

About this variant

This variant has 2535 sample genotypes, is associated with 25 phenotypes and is mentioned in 8 citations.

Variant displays