Source: ALL

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 100529261
Gene Symbol: CHURC1-FNTB
CHURC1-FNTB
CUI: C0005890
Disease: Body Height
Body Height 		0.100 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370

2019
Entrez Id: 100529261
Gene Symbol: CHURC1-FNTB
CHURC1-FNTB
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: 100529261
Gene Symbol: CHURC1-FNTB
CHURC1-FNTB
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: 100529261
Gene Symbol: CHURC1-FNTB
CHURC1-FNTB
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio 		0.100 GeneticVariation GWASCAT Meta-analysis of genome-wide association studies for body fat distribution in 694 649 individuals of European ancestry. 30239722

2019
Entrez Id: 100529261
Gene Symbol: CHURC1-FNTB
CHURC1-FNTB
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.100 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370

2019
Entrez Id: 100529261
Gene Symbol: CHURC1-FNTB
CHURC1-FNTB
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.100 GeneticVariation GWASCAT Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. 29403010

2018
Entrez Id: 100529261
Gene Symbol: CHURC1-FNTB
CHURC1-FNTB
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result) 		0.100 GeneticVariation GWASCAT Genome-wide Trans-ethnic Meta-analysis Identifies Seven Genetic Loci Influencing Erythrocyte Traits and a Role for RBPMS in Erythropoiesis. 28017375

2017
Entrez Id: 100529261
Gene Symbol: CHURC1-FNTB
CHURC1-FNTB
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.100 GeneticVariation GWASCAT Genome-wide Trans-ethnic Meta-analysis Identifies Seven Genetic Loci Influencing Erythrocyte Traits and a Role for RBPMS in Erythropoiesis. 28017375

2017
Entrez Id: 100529261
Gene Symbol: CHURC1-FNTB
CHURC1-FNTB
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.100 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252

2016
Entrez Id: 100529261
Gene Symbol: CHURC1-FNTB
CHURC1-FNTB
CUI: C0200665
Disease: Platelet mean volume determination (procedure)
Platelet mean volume determination (procedure) 		0.100 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252

2016
Entrez Id: 100529261
Gene Symbol: CHURC1-FNTB
CHURC1-FNTB
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result) 		0.100 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252

2016
Entrez Id: 100529261
Gene Symbol: CHURC1-FNTB
CHURC1-FNTB
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.100 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252

2016
Entrez Id: 100529261
Gene Symbol: CHURC1-FNTB
CHURC1-FNTB
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.100 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252

2016
Entrez Id: 100529261
Gene Symbol: CHURC1-FNTB
CHURC1-FNTB
CUI: C1318315
Disease: Serum zinc measurement
Serum zinc measurement 		0.100 GeneticVariation GWASCAT Genome-wide association study identifies loci affecting blood copper, selenium and zinc. 23720494

2013
Entrez Id: 100529261
Gene Symbol: CHURC1-FNTB
CHURC1-FNTB
CUI: C1318315
Disease: Serum zinc measurement
Serum zinc measurement 		0.100 GeneticVariation GWASDB Genome-wide association study identifies loci affecting blood copper, selenium and zinc. 23720494

2013
Entrez Id: 100529261
Gene Symbol: CHURC1-FNTB
CHURC1-FNTB
CUI: C0200635
Disease: Lymphocyte Count measurement
Lymphocyte Count measurement 		0.100 GeneticVariation GWASDB The combination of a genome-wide association study of lymphocyte count and analysis of gene expression data reveals novel asthma candidate genes. 22286170

2012
Entrez Id: 100529261
Gene Symbol: CHURC1-FNTB
CHURC1-FNTB
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.100 GeneticVariation GWASDB Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. 23063622

2012
Entrez Id: 100529261
Gene Symbol: CHURC1-FNTB
CHURC1-FNTB
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.100 GeneticVariation GWASDB Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. 23063622

2012
Entrez Id: 100529261
Gene Symbol: CHURC1-FNTB
CHURC1-FNTB
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.100 GeneticVariation GWASDB Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. 23063622

2012
Entrez Id: 100529261
Gene Symbol: CHURC1-FNTB
CHURC1-FNTB
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement 		0.100 GeneticVariation GWASDB Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. 23063622

2012
Entrez Id: 100529261
Gene Symbol: CHURC1-FNTB
CHURC1-FNTB
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.100 GeneticVariation GWASCAT Seventy-five genetic loci influencing the human red blood cell. 23222517

2012
Entrez Id: 100529261
Gene Symbol: CHURC1-FNTB
CHURC1-FNTB
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.100 GeneticVariation GWASDB Seventy-five genetic loci influencing the human red blood cell. 23222517

2012
Entrez Id: 100529261
Gene Symbol: CHURC1-FNTB
CHURC1-FNTB
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.100 GeneticVariation GWASDB Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. 19862010

2009
Entrez Id: 100529261
Gene Symbol: CHURC1-FNTB
CHURC1-FNTB
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result) 		0.100 GeneticVariation GWASCAT Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. 19862010

2009
Entrez Id: 100529261
Gene Symbol: CHURC1-FNTB
CHURC1-FNTB
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result) 		0.100 GeneticVariation GWASDB Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. 19862010

2009