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/G|Ancestral: A|Ambiguity code: R|MAF: 0.26 (G)
Location

This variant maps to 7 genomic locations; None selected

Evidence status

Synonyms
HGVS name

None

Genotyping chips

This variant has assays on 7 chips - Show

About this variant

This variant has 3691 sample genotypes, is associated with 7 phenotypes and is mentioned in 7 citations.

Variant displays