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: 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: rs10464870
rs10464870
Entrez Id: 137196
Gene Symbol: CCDC26
CCDC26
CUI: C1621958
Disease:
Glioblastoma Multiforme 		0.010 GeneticVariation BEFREE We identified LIG4 rs7325927 and BTBD2 rs11670188 as predictors of STS in GBM and CCDC26 rs10464870 and rs891835, HMGA2 rs1563834, and RTEL1 rs2297440 as predictors of LTS. 20368557 2010
dbSNP: rs10464870
rs10464870
Entrez Id: 137196
Gene Symbol: CCDC26
CCDC26
CUI: C0017636
Disease:
Glioblastoma 		0.010 GeneticVariation BEFREE We identified LIG4 rs7325927 and BTBD2 rs11670188 as predictors of STS in GBM and CCDC26 rs10464870 and rs891835, HMGA2 rs1563834, and RTEL1 rs2297440 as predictors of LTS. 20368557 2010
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