CEP112, centrosomal protein 112, 201134

N. diseases: 10; N. variants: 11
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs8074751
rs8074751
Entrez Id: 201134
Gene Symbol: CEP112
CEP112
CUI: C1263846
Disease:
Attention deficit hyperactivity disorder 		0.800 GeneticVariation GWASCAT Family-based genome-wide association scan of attention-deficit/hyperactivity disorder. 20732626 2010
dbSNP: rs8074751
rs8074751
Entrez Id: 201134
Gene Symbol: CEP112
CEP112
CUI: C1263846
Disease:
Attention deficit hyperactivity disorder 		0.800 GeneticVariation GWASDB Family-based genome-wide association scan of attention-deficit/hyperactivity disorder. 20732626 2010
dbSNP: rs117525469
rs117525469
Entrez Id: 201134
Gene Symbol: CEP112
CEP112
CUI: C0005890
Disease:
Body Height 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs232094
rs232094
Entrez Id: 201134
Gene Symbol: CEP112
CEP112
CUI: C0005890
Disease:
Body Height 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs147178973
rs147178973
Entrez Id: 201134;105371867
Gene Symbol: CEP112;LOC105371867
CEP112;LOC105371867
CUI: C0201973
Disease:
Creatine kinase measurement 		0.700 GeneticVariation GWASCAT Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. 29403010 2018
dbSNP: rs7213215
rs7213215
Entrez Id: 201134
Gene Symbol: CEP112
CEP112
CUI: C2985280
Disease:
Blood Protein Measurement 		G 0.700 GeneticVariation GWASCAT Genomic atlas of the human plasma proteome. 29875488 2018
dbSNP: rs746627
rs746627
Entrez Id: 201134
Gene Symbol: CEP112
CEP112
CUI: C0005938
Disease:
Bone Density 		T 0.700 GeneticVariation GWASCAT Life-Course Genome-wide Association Study Meta-analysis of Total Body BMD and Assessment of Age-Specific Effects. 29304378 2018
dbSNP: rs9891968
rs9891968
Entrez Id: 201134
Gene Symbol: CEP112
CEP112
CUI: C2985280
Disease:
Blood Protein Measurement 		A 0.700 GeneticVariation GWASCAT Genomic atlas of the human plasma proteome. 29875488 2018
dbSNP: rs9972944
rs9972944
Entrez Id: 201134
Gene Symbol: CEP112
CEP112
CUI: C0005938
Disease:
Bone Density 		A 0.700 GeneticVariation GWASCAT Life-Course Genome-wide Association Study Meta-analysis of Total Body BMD and Assessment of Age-Specific Effects. 29304378 2018
dbSNP: rs9910950
rs9910950
Entrez Id: 201134
Gene Symbol: CEP112
CEP112
CUI: C0201534
Disease:
Antiphospholipid antibodies measurement 		0.700 GeneticVariation GWASCAT Antiphospholipid antibodies in a large population-based cohort: genome-wide associations and effects on monocyte gene expression. 27098658 2016
dbSNP: rs181929163
rs181929163
Entrez Id: 201134
Gene Symbol: CEP112
CEP112
CUI: C0202202
Disease:
Protein measurement 		0.700 GeneticVariation GWASCAT Imputation of variants from the 1000 Genomes Project modestly improves known associations and can identify low-frequency variant-phenotype associations undetected by HapMap based imputation. 23696881 2013
dbSNP: rs16958921
rs16958921
Entrez Id: 201134
Gene Symbol: CEP112
CEP112
CUI: C0027404
Disease:
Narcolepsy 		0.700 GeneticVariation GWASDB Genome-wide association database developed in the Japanese Integrated Database Project. 19629137 2009