Source: GWASCAT

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 137196
Gene Symbol: CCDC26
CCDC26
CUI: C0017638
Disease: Glioma
Glioma
0.500 GeneticVariation GWASCAT Sex-specific glioma genome-wide association study identifies new risk locus at 3p21.31 in females, and finds sex-differences in risk at 8q24.21. 29743610

2018

Entrez Id: 137196
Gene Symbol: CCDC26
CCDC26
CUI: C0017638
Disease: Glioma
Glioma
0.500 GeneticVariation GWASCAT Genome-wide association study of glioma subtypes identifies specific differences in genetic susceptibility to glioblastoma and non-glioblastoma tumors. 28346443

2017

Entrez Id: 137196
Gene Symbol: CCDC26
CCDC26
CUI: C0017638
Disease: Glioma
Glioma
0.500 GeneticVariation GWASCAT Genome-wide association study identifies multiple susceptibility loci for glioma. 26424050

2015

Entrez Id: 137196
Gene Symbol: CCDC26
CCDC26
CUI: C0017638
Disease: Glioma
Glioma
0.500 GeneticVariation GWASCAT Chromosome 7p11.2 (EGFR) variation influences glioma risk. 21531791

2011

Entrez Id: 137196
Gene Symbol: CCDC26
CCDC26
CUI: C0017638
Disease: Glioma
Glioma
0.500 GeneticVariation GWASCAT We identified five risk loci for glioma at 5p15.33 (rs2736100, TERT; P = 1.50 x 10(-17)), 8q24.21 (rs4295627, CCDC26; P = 2.34 x 10(-18)), 9p21.3 (rs4977756, CDKN2A-CDKN2B; P = 7.24 x 10(-15)), 20q13.33 (rs6010620, RTEL1; P = 2.52 x 10(-12)) and 11q23.3 (rs498872, PHLDB1; P = 1.07 x 10(-8)). 19578367

2009

Entrez Id: 137196
Gene Symbol: CCDC26
CCDC26
CUI: C0017636
Disease: Glioblastoma
Glioblastoma
0.140 GeneticVariation GWASCAT Age-specific genome-wide association study in glioblastoma identifies increased proportion of 'lower grade glioma'-like features associated with younger age. 30152087

2018

Entrez Id: 137196
Gene Symbol: CCDC26
CCDC26
CUI: C1621958
Disease: Glioblastoma Multiforme
Glioblastoma Multiforme
0.140 GeneticVariation GWASCAT Age-specific genome-wide association study in glioblastoma identifies increased proportion of 'lower grade glioma'-like features associated with younger age. 30152087

2018

Entrez Id: 137196
Gene Symbol: CCDC26
CCDC26
CUI: C0017636
Disease: Glioblastoma
Glioblastoma
0.140 GeneticVariation GWASCAT Genome-wide association study of glioma subtypes identifies specific differences in genetic susceptibility to glioblastoma and non-glioblastoma tumors. 28346443

2017

Entrez Id: 137196
Gene Symbol: CCDC26
CCDC26
CUI: C1621958
Disease: Glioblastoma Multiforme
Glioblastoma Multiforme
0.140 GeneticVariation GWASCAT Genome-wide association study of glioma subtypes identifies specific differences in genetic susceptibility to glioblastoma and non-glioblastoma tumors. 28346443

2017

Entrez Id: 137196
Gene Symbol: CCDC26
CCDC26
CUI: C0005890
Disease: Body Height
Body Height
0.100 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370

2019

Entrez Id: 137196
Gene Symbol: CCDC26
CCDC26
CUI: C0013595
Disease: Eczema
Eczema
0.100 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370

2019

Entrez Id: 137196
Gene Symbol: CCDC26
CCDC26
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement
0.100 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370

2019

Entrez Id: 137196
Gene Symbol: CCDC26
CCDC26
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure
0.100 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370

2019

Entrez Id: 137196
Gene Symbol: CCDC26
CCDC26
CUI: C0042834
Disease: Vital capacity
Vital capacity
0.100 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370

2019

Entrez Id: 137196
Gene Symbol: CCDC26
CCDC26
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.100 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370

2019

Entrez Id: 137196
Gene Symbol: CCDC26
CCDC26
Finding of Mean Corpuscular Hemoglobin
0.100 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370

2019

Entrez Id: 137196
Gene Symbol: CCDC26
CCDC26
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate
0.100 GeneticVariation GWASCAT Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. 29403010

2018

Entrez Id: 137196
Gene Symbol: CCDC26
CCDC26
Precursor B-Cell Lymphoblastic Leukemia-Lymphoma
0.100 GeneticVariation GWASCAT Genome-wide association study identifies susceptibility loci for B-cell childhood acute lymphoblastic leukemia. 29632299

2018

Entrez Id: 137196
Gene Symbol: CCDC26
CCDC26
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure
0.100 GeneticVariation GWASCAT Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. 29403010

2018

Entrez Id: 137196
Gene Symbol: CCDC26
CCDC26
CUI: C0200633
Disease: Neutrophil count (procedure)
Neutrophil count (procedure)
0.100 GeneticVariation GWASCAT Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. 29403010

2018

Entrez Id: 137196
Gene Symbol: CCDC26
CCDC26
CUI: C0200637
Disease: Monocyte count procedure
Monocyte count procedure
0.100 GeneticVariation GWASCAT Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. 29403010

2018

Entrez Id: 137196
Gene Symbol: CCDC26
CCDC26
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.100 GeneticVariation GWASCAT Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. 29403010

2018

Entrez Id: 137196
Gene Symbol: CCDC26
CCDC26
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test)
0.100 GeneticVariation GWASCAT Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. 29403010

2018

Entrez Id: 137196
Gene Symbol: CCDC26
CCDC26
Creatinine measurement, serum (procedure)
0.100 GeneticVariation GWASCAT Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. 29403010

2018

Entrez Id: 137196
Gene Symbol: CCDC26
CCDC26
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
Adolescent idiopathic scoliosis
0.100 GeneticVariation GWASCAT The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease. 30019117

2018