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
T/A|Ancestral: T|Ambiguity code: W|MAF: 0.02 (A)
Location

This variant maps to 2 genomic locations; None selected

Evidence status

Clinical significance

Synonyms

This variant has 5 synonyms - Show

HGVS name

None

Genotyping chips

This variant has assays on 4 chips - Show

About this variant

This variant has 2775 sample genotypes, is associated with 8 phenotypes and is mentioned in 15 citations.

Variant displays