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/A | Ancestral: G | Ambiguity code: R | MAF: 0.09 (A)

This variant maps to 7 genomic locations; None selected

Evidence status

HGVS name


Genotyping chips

This variant has assays on 9 chips - Show

About this variant

This variant has 4896 sample genotypes, is associated with 7 phenotypes and is mentioned in 466 citations.

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