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
G/A/T|Ancestral: G|Ambiguity code: D|MAF: < 0.01 (A)
Location

This variant maps to 7 genomic locations; None selected

Evidence status

Clinical significance

Synonyms

This variant has 6 synonyms - Show

HGVS name

None

Genotyping chips

This variant has assays on: Illumina_HumanOmni5

About this variant

This variant has 2541 sample genotypes, is associated with 21 phenotypes and is mentioned in 2 citations.

Variant displays