CCDC26, CCDC26 long non-coding RNA, 137196

N. diseases: 60; N. variants: 111
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs55705857
rs55705857
Entrez Id: 137196
Gene Symbol: CCDC26
CCDC26
CUI: C0017636
Disease:
Glioblastoma 		G 0.710 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
dbSNP: rs55705857
rs55705857
Entrez Id: 137196
Gene Symbol: CCDC26
CCDC26
CUI: C0017636
Disease:
Glioblastoma 		0.710 GeneticVariation BEFREE Analysis by glioma subtype showed the association with rs55705857 confined to non-glioblastoma multiforme (non-GBM) tumours (P = 1.07 × 10(-67)). 23399484 2013
dbSNP: rs10098310
rs10098310
Entrez Id: 137196
Gene Symbol: CCDC26
CCDC26
CUI: C0200637
Disease:
Monocyte count procedure 		A 0.700 GeneticVariation GWASCAT Multiple loci are associated with white blood cell phenotypes. 21738480 2011
dbSNP: rs10098310
rs10098310
Entrez Id: 137196
Gene Symbol: CCDC26
CCDC26
CUI: C0750880
Disease:
Monocyte count result 		A 0.700 GeneticVariation GWASCAT Multiple loci are associated with white blood cell phenotypes. 21738480 2011
dbSNP: rs10098310
rs10098310
Entrez Id: 137196
Gene Symbol: CCDC26
CCDC26
CUI: C0023508
Disease:
White Blood Cell Count procedure 		0.700 GeneticVariation GWASDB Multiple loci are associated with white blood cell phenotypes. 21738480 2011
dbSNP: rs10100356
rs10100356
Entrez Id: 137196
Gene Symbol: CCDC26
CCDC26
CUI: C0200641
Disease:
Blood basophil count (lab test) 		0.700 GeneticVariation GWASCAT Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. 29403010 2018
dbSNP: rs10107630
rs10107630
Entrez Id: 137196
Gene Symbol: CCDC26
CCDC26
CUI: C0014772
Disease:
Red Blood Cell Count measurement 		T 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs10107630
rs10107630
Entrez Id: 137196
Gene Symbol: CCDC26
CCDC26
CUI: C1261502
Disease:
Finding of Mean Corpuscular Hemoglobin 		T 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs10107630
rs10107630
Entrez Id: 137196
Gene Symbol: CCDC26
CCDC26
CUI: C0524587
Disease:
Mean Corpuscular Volume (result) 		T 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs1030608
rs1030608
Entrez Id: 137196
Gene Symbol: CCDC26
CCDC26
CUI: C0008924
Disease:
Cleft upper lip 		0.700 GeneticVariation GWASDB Genome-wide meta-analyses of nonsyndromic cleft lip with or without cleft palate identify six new risk loci. 22863734 2012
dbSNP: rs1030609
rs1030609
Entrez Id: 137196
Gene Symbol: CCDC26
CCDC26
CUI: C0008924
Disease:
Cleft upper lip 		0.700 GeneticVariation GWASDB Genome-wide meta-analyses of nonsyndromic cleft lip with or without cleft palate identify six new risk loci. 22863734 2012
dbSNP: rs10464870
rs10464870
Entrez Id: 137196
Gene Symbol: CCDC26
CCDC26
CUI: C0017638
Disease:
Glioma 		0.700 GeneticVariation GWASDB Chromosome 7p11.2 (EGFR) variation influences glioma risk. 21531791 2011
dbSNP: rs10464870
rs10464870
Entrez Id: 137196
Gene Symbol: CCDC26
CCDC26
CUI: C0017638
Disease:
Glioma 		G 0.700 GeneticVariation GWASDB Genome-wide association study identifies five susceptibility loci for glioma. 19578367 2009
dbSNP: rs10481172
rs10481172
Entrez Id: 137196
Gene Symbol: CCDC26
CCDC26
CUI: C0200638
Disease:
Eosinophil count procedure 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs10808576
rs10808576
Entrez Id: 137196
Gene Symbol: CCDC26
CCDC26
CUI: C0008924
Disease:
Cleft upper lip 		0.700 GeneticVariation GWASDB Genome-wide meta-analyses of nonsyndromic cleft lip with or without cleft palate identify six new risk loci. 22863734 2012
dbSNP: rs10956445
rs10956445
Entrez Id: 137196
Gene Symbol: CCDC26
CCDC26
CUI: C3495559
Disease:
Juvenile arthritis 		C 0.700 GeneticVariation GWASCAT Genome-wide data reveal novel genes for methotrexate response in a large cohort of juvenile idiopathic arthritis cases. 24709693 2014
dbSNP: rs10956453
rs10956453
Entrez Id: 137196
Gene Symbol: CCDC26
CCDC26
CUI: C0008924
Disease:
Cleft upper lip 		0.700 GeneticVariation GWASDB Key susceptibility locus for nonsyndromic cleft lip with or without cleft palate on chromosome 8q24. 19270707 2009
dbSNP: rs10956483
rs10956483
Entrez Id: 137196
Gene Symbol: CCDC26
CCDC26
CUI: C0200638
Disease:
Eosinophil count procedure 		C 0.700 GeneticVariation GWASDB Identification of nine novel loci associated with white blood cell subtypes in a Japanese population. 21738478 2011
dbSNP: rs10956483
rs10956483
Entrez Id: 137196
Gene Symbol: CCDC26
CCDC26
CUI: C0750880
Disease:
Monocyte count result 		C 0.700 GeneticVariation GWASCAT Identification of nine novel loci associated with white blood cell subtypes in a Japanese population. 21738478 2011
dbSNP: rs10956483
rs10956483
Entrez Id: 137196
Gene Symbol: CCDC26
CCDC26
CUI: C0200637
Disease:
Monocyte count procedure 		C 0.700 GeneticVariation GWASCAT Identification of nine novel loci associated with white blood cell subtypes in a Japanese population. 21738478 2011
dbSNP: rs11327184
rs11327184
Entrez Id: 137196
Gene Symbol: CCDC26
CCDC26
CUI: C0200638
Disease:
Eosinophil count procedure 		A 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs11327184
rs11327184
Entrez Id: 137196
Gene Symbol: CCDC26
CCDC26
CUI: C0200641
Disease:
Blood basophil count (lab test) 		A 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs11327184
rs11327184
Entrez Id: 137196
Gene Symbol: CCDC26
CCDC26
CUI: C0750880
Disease:
Monocyte count result 		A 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs11327184
rs11327184
Entrez Id: 137196
Gene Symbol: CCDC26
CCDC26
CUI: C0200637
Disease:
Monocyte count procedure 		A 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs11506137
rs11506137
Entrez Id: 137196
Gene Symbol: CCDC26
CCDC26
CUI: C0008924
Disease:
Cleft upper lip 		0.700 GeneticVariation GWASDB Key susceptibility locus for nonsyndromic cleft lip with or without cleft palate on chromosome 8q24. 19270707 2009