Source: GWASCAT

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 81037
Gene Symbol: CLPTM1L
CLPTM1L
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
Adenocarcinoma of lung (disorder) 		0.460 GeneticVariation GWASCAT Identification of risk loci and a polygenic risk score for lung cancer: a large-scale prospective cohort study in Chinese populations. 31326317

2019
Entrez Id: 81037
Gene Symbol: CLPTM1L
CLPTM1L
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
Adenocarcinoma of lung (disorder) 		0.460 GeneticVariation GWASCAT Lung Cancer Risk in Never-Smokers of European Descent is Associated With Genetic Variation in the 5p15.33 TERT-CLPTM1Ll Region. 31009812

2019
Entrez Id: 81037
Gene Symbol: CLPTM1L
CLPTM1L
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
Adenocarcinoma of lung (disorder) 		0.460 GeneticVariation GWASCAT A genome-wide association study of lung cancer identifies a region of chromosome 5p15 associated with risk for adenocarcinoma. 19836008

2009
Entrez Id: 81037
Gene Symbol: CLPTM1L
CLPTM1L
CUI: C0751676
Disease: Basal Cell Cancer
Basal Cell Cancer 		0.100 GeneticVariation GWASCAT Germline sequence variants in TGM3 and RGS22 confer risk of basal cell carcinoma. 24403052

2014
Entrez Id: 81037
Gene Symbol: CLPTM1L
CLPTM1L
CUI: C0751676
Disease: Basal Cell Cancer
Basal Cell Cancer 		0.100 GeneticVariation GWASCAT Combined analysis of keratinocyte cancers identifies novel genome-wide loci. 31174203

2019
Entrez Id: 81037
Gene Symbol: CLPTM1L
CLPTM1L
CUI: C0751676
Disease: Basal Cell Cancer
Basal Cell Cancer 		0.100 GeneticVariation GWASCAT Genome-wide association study identifies 14 novel risk alleles associated with basal cell carcinoma. 27539887

2016
Entrez Id: 81037
Gene Symbol: CLPTM1L
CLPTM1L
CUI: C0751676
Disease: Basal Cell Cancer
Basal Cell Cancer 		0.100 GeneticVariation GWASCAT Sequence variants at the TERT-CLPTM1L locus associate with many cancer types. 19151717

2009
Entrez Id: 81037
Gene Symbol: CLPTM1L
CLPTM1L
CUI: C0751676
Disease: Basal Cell Cancer
Basal Cell Cancer 		0.100 GeneticVariation GWASCAT New basal cell carcinoma susceptibility loci. 25855136

2015
Entrez Id: 81037
Gene Symbol: CLPTM1L
CLPTM1L
CUI: C0007117
Disease: Basal cell carcinoma
Basal cell carcinoma 		0.100 GeneticVariation GWASCAT Genome-wide association study identifies 14 novel risk alleles associated with basal cell carcinoma. 27539887

2016
Entrez Id: 81037
Gene Symbol: CLPTM1L
CLPTM1L
CUI: C0007117
Disease: Basal cell carcinoma
Basal cell carcinoma 		0.100 GeneticVariation GWASCAT New basal cell carcinoma susceptibility loci. 25855136

2015
Entrez Id: 81037
Gene Symbol: CLPTM1L
CLPTM1L
CUI: C0007117
Disease: Basal cell carcinoma
Basal cell carcinoma 		0.100 GeneticVariation GWASCAT Sequence variants at the TERT-CLPTM1L locus associate with many cancer types. 19151717

2009
Entrez Id: 81037
Gene Symbol: CLPTM1L
CLPTM1L
CUI: C0007117
Disease: Basal cell carcinoma
Basal cell carcinoma 		0.100 GeneticVariation GWASCAT Combined analysis of keratinocyte cancers identifies novel genome-wide loci. 31174203

2019
Entrez Id: 81037
Gene Symbol: CLPTM1L
CLPTM1L
CUI: C0007117
Disease: Basal cell carcinoma
Basal cell carcinoma 		0.100 GeneticVariation GWASCAT Germline sequence variants in TGM3 and RGS22 confer risk of basal cell carcinoma. 24403052

2014
Entrez Id: 81037
Gene Symbol: CLPTM1L
CLPTM1L
CUI: C0206710
Disease: Basal Cell Neoplasm
Basal Cell Neoplasm 		0.100 GeneticVariation GWASCAT New basal cell carcinoma susceptibility loci. 25855136

2015
Entrez Id: 81037
Gene Symbol: CLPTM1L
CLPTM1L
CUI: C0206710
Disease: Basal Cell Neoplasm
Basal Cell Neoplasm 		0.100 GeneticVariation GWASCAT Germline sequence variants in TGM3 and RGS22 confer risk of basal cell carcinoma. 24403052

2014
Entrez Id: 81037
Gene Symbol: CLPTM1L
CLPTM1L
CUI: C0206710
Disease: Basal Cell Neoplasm
Basal Cell Neoplasm 		0.100 GeneticVariation GWASCAT Genome-wide association study identifies 14 novel risk alleles associated with basal cell carcinoma. 27539887

2016
Entrez Id: 81037
Gene Symbol: CLPTM1L
CLPTM1L
CUI: C0206710
Disease: Basal Cell Neoplasm
Basal Cell Neoplasm 		0.100 GeneticVariation GWASCAT Combined analysis of keratinocyte cancers identifies novel genome-wide loci. 31174203

2019
Entrez Id: 81037
Gene Symbol: CLPTM1L
CLPTM1L
CUI: C0206710
Disease: Basal Cell Neoplasm
Basal Cell Neoplasm 		0.100 GeneticVariation GWASCAT Sequence variants at the TERT-CLPTM1L locus associate with many cancer types. 19151717

2009
Entrez Id: 81037
Gene Symbol: CLPTM1L
CLPTM1L
CUI: C1704272
Disease: Benign Prostatic Hyperplasia
Benign Prostatic Hyperplasia 		0.100 GeneticVariation GWASCAT Genome-wide associations for benign prostatic hyperplasia reveal a genetic correlation with serum levels of PSA. 30410027

2018
Entrez Id: 81037
Gene Symbol: CLPTM1L
CLPTM1L
CUI: C0699885
Disease: Carcinoma of bladder
Carcinoma of bladder 		0.100 GeneticVariation GWASCAT A multi-stage genome-wide association study of bladder cancer identifies multiple susceptibility loci. 20972438

2010
Entrez Id: 81037
Gene Symbol: CLPTM1L
CLPTM1L
CUI: C0699885
Disease: Carcinoma of bladder
Carcinoma of bladder 		0.100 GeneticVariation GWASCAT Genome-wide association study identifies multiple loci associated with bladder cancer risk. 24163127

2014
Entrez Id: 81037
Gene Symbol: CLPTM1L
CLPTM1L
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung 		0.200 GeneticVariation GWASCAT Lung Cancer Risk in Never-Smokers of European Descent is Associated With Genetic Variation in the 5p15.33 TERT-CLPTM1Ll Region. 31009812

2019
Entrez Id: 81037
Gene Symbol: CLPTM1L
CLPTM1L
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung 		0.200 GeneticVariation GWASCAT Common 5p15.33 and 6p21.33 variants influence lung cancer risk. 18978787

2008
Entrez Id: 81037
Gene Symbol: CLPTM1L
CLPTM1L
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung 		0.200 GeneticVariation GWASCAT Large-scale association analysis identifies new lung cancer susceptibility loci and heterogeneity in genetic susceptibility across histological subtypes. 28604730

2017
Entrez Id: 81037
Gene Symbol: CLPTM1L
CLPTM1L
CUI: C0023434
Disease: Chronic Lymphocytic Leukemia
Chronic Lymphocytic Leukemia 		0.100 GeneticVariation GWASCAT A genome-wide association study identifies multiple susceptibility loci for chronic lymphocytic leukemia. 24292274

2014