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/C|Ancestral: T|Ambiguity code: Y|MAF: < 0.01 (C)
Location

This variant maps to 2 genomic locations; None selected

Evidence status

Clinical significance

Synonyms

This variant has 7 synonyms - Show

HGVS name

None

Genotyping chips

This variant has assays on: Illumina_ImmunoChip, Illumina_HumanOmni1-Quad

About this variant

This variant has 2748 sample genotypes, is associated with 10 phenotypes and is mentioned in 4 citations.

Variant displays