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|Ambiguity code: Y|MAF: 0.29 (C)
Location

This variant maps to 4 genomic locations; None selected

Evidence status

HGVS name

None

Genotyping chips

This variant has assays on 4 chips - Show

About this variant

This variant has 3962 sample genotypes, is associated with 4 phenotypes and is mentioned in 7 citations.

Variant displays