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

A/G|Ambiguity code: R|MAF: 0.11 (G)

This variant maps to 7 genomic locations; None selected

Evidence status


Archive dbSNP rs59204384, rs113380831

HGVS name


Genotyping chips

This variant has assays on: Affy GenomeWideSNP_6.0, Affy GeneChip 500K, Illumina_HumanOmni5

About this variant

This variant has 3694 sample genotypes and is mentioned in 2 citations.

Variant displays