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
C/T|Ancestral: C|Ambiguity code: Y|MAF: 0.04 (T)
Location

This variant maps to 7 genomic locations; None selected

Evidence status

Synonyms

Archive dbSNP rs116138574, rs117316167

HGVS name

None

Genotyping chips

This variant has assays on 7 chips - Show

About this variant

This variant has 3691 sample genotypes, is associated with 7 phenotypes and is mentioned in 2 citations.

Variant displays