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/G|Ancestral: T|Ambiguity code: K|MAF: 0.01 (G)
Location

This variant maps to 2 genomic locations; None selected

Evidence status

HGVS name

None

Genotyping chips

This variant has assays on: Illumina_HumanOmni1-Quad

About this variant

This variant overlaps 1 regulatory feature, has 2504 sample genotypes and is mentioned in 2 citations.

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