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: 0.41 (C)
Location

This variant maps to 2 genomic locations; None selected

Evidence status

Synonyms

Archive dbSNP rs3824859

HGVS name

None

Genotyping chips

This variant has assays on: Illumina_HumanOmni2.5, Illumina_HumanOmni1-Quad

About this variant

This variant has 2505 sample genotypes and is mentioned in 42 citations.

Variant displays