rs11756438

This is a intron variant variant in the CEP85L gene.

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GWAS Catalog Trait Associations (2)

Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.

QT interval

Newton-Cheh C et al. “Common variants at ten loci influence QT interval duration in the QTGEN Study.” Nature Genetics 41(4):399-406 (2009)

Allele A

OR 1.40

p 5.0e-22

N 13,685

Large GWAS

European

attention deficit hyperactivity disorder, bipolar disorder

van Hulzen KJE et al. “Genetic Overlap Between Attention-Deficit/Hyperactivity Disorder and Bipolar Disorder: Evidence From Genome-wide Association Study Meta-analysis.” Biological Psychiatry 82(9):634-641 (2017)

Allele A

OR 1.10

p 4.0e-8

N 35,622

Meta-analysisLarge GWAS

multi-ancestry

About CEP85L

The protein encoded by this gene was identified as a breast cancer antigen. Nothing more is known of its function at this time. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2010]

View all CEP85L variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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