Source: GWASCAT

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2736100
rs2736100
CUI: C0017638
Disease: Glioma
Glioma
C 0.900 GeneticVariation GWASCAT Two novel genetic variants in the STK38L and RAB27A genes are associated with glioma susceptibility. 30714141

2019

dbSNP: rs2736100
rs2736100
CUI: C0017638
Disease: Glioma
Glioma
C 0.900 GeneticVariation GWASCAT Variants near TERT and TERC influencing telomere length are associated with high-grade glioma risk. 24908248

2014

dbSNP: rs2736100
rs2736100
CUI: C0017638
Disease: Glioma
Glioma
G 0.900 GeneticVariation GWASCAT Genome-wide association study of glioma and meta-analysis. 22886559

2012

dbSNP: rs2736100
rs2736100
CUI: C0017638
Disease: Glioma
Glioma
0.900 GeneticVariation GWASCAT Chromosome 7p11.2 (EGFR) variation influences glioma risk. 21531791

2011

dbSNP: rs2736100
rs2736100
CUI: C0017638
Disease: Glioma
Glioma
0.900 GeneticVariation GWASCAT Combinations of newly confirmed Glioma-Associated loci link regions on chromosomes 1 and 9 to increased disease risk. 21827660

2011

dbSNP: rs2736100
rs2736100
CUI: C0017638
Disease: Glioma
Glioma
G 0.900 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

dbSNP: rs2736100
rs2736100
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
Adenocarcinoma of lung (disorder)
G 0.880 GeneticVariation GWASCAT Association of variations in HLA class II and other loci with susceptibility to EGFR-mutated lung adenocarcinoma. 27501781

2016

dbSNP: rs2736100
rs2736100
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
Adenocarcinoma of lung (disorder)
G 0.880 GeneticVariation GWASCAT Since most women in Asia do not smoke, we conducted a genome-wide association study of lung adenocarcinoma in never-smoking females (584 cases, 585 controls) among Han Chinese in Taiwan and found that the most significant association was for rs2736100 on chromosome 5p15.33 (p = 1.30 x 10(-11)). 20700438

2010

dbSNP: rs2736100
rs2736100
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
Adenocarcinoma of lung (disorder)
C 0.880 GeneticVariation GWASCAT The combined analyses identified two susceptibility loci for lung adenocarcinoma: TERT (rs2736100, combined P = 2.91 × 10⁻¹¹), odds ratio (OR) = 1.27) and TP63 (rs10937405, combined P = 7.26 × 10⁻¹²), OR = 1.31). 20871597

2010

dbSNP: rs2736100
rs2736100
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
Adenocarcinoma of lung (disorder)
G 0.880 GeneticVariation GWASCAT A genome-wide association study of lung cancer identifies a region of chromosome 5p15 associated with risk for adenocarcinoma. 19836008

2009

dbSNP: rs2736100
rs2736100
CUI: C1800706
Disease: Idiopathic Pulmonary Fibrosis
Idiopathic Pulmonary Fibrosis
A 0.840 GeneticVariation GWASCAT A genome-wide association study identifies an association of a common variant in TERT with susceptibility to idiopathic pulmonary fibrosis. 18835860

2008

dbSNP: rs2736100
rs2736100
CUI: C0206062
Disease: Lung Diseases, Interstitial
Lung Diseases, Interstitial
A 0.810 GeneticVariation GWASCAT Genome-wide association study identifies multiple susceptibility loci for pulmonary fibrosis. 23583980

2013

dbSNP: rs2736100
rs2736100
CUI: C1336708
Disease: Testicular Germ Cell Tumor
Testicular Germ Cell Tumor
A 0.800 GeneticVariation GWASCAT Meta-analysis of five genome-wide association studies identifies multiple new loci associated with testicular germ cell tumor. 28604732

2017

dbSNP: rs2736100
rs2736100
CUI: C1336708
Disease: Testicular Germ Cell Tumor
Testicular Germ Cell Tumor
A 0.800 GeneticVariation GWASCAT Identification of 19 new risk loci and potential regulatory mechanisms influencing susceptibility to testicular germ cell tumor. 28604728

2017

dbSNP: rs2736100
rs2736100
CUI: C0085136
Disease: Central Nervous System Neoplasms
Central Nervous System Neoplasms
C 0.800 GeneticVariation GWASCAT Variants near TERT and TERC influencing telomere length are associated with high-grade glioma risk. 24908248

2014

dbSNP: rs2736100
rs2736100
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung
G 0.800 GeneticVariation GWASCAT Genome-wide association analysis identifies new lung cancer susceptibility loci in never-smoking women in Asia. 23143601

2012

dbSNP: rs2736100
rs2736100
CUI: C0085136
Disease: Central Nervous System Neoplasms
Central Nervous System Neoplasms
G 0.800 GeneticVariation GWASCAT Genome-wide association study of glioma and meta-analysis. 22886559

2012

dbSNP: rs2736100
rs2736100
CUI: C0085136
Disease: Central Nervous System Neoplasms
Central Nervous System Neoplasms
0.800 GeneticVariation GWASCAT Combinations of newly confirmed Glioma-Associated loci link regions on chromosomes 1 and 9 to increased disease risk. 21827660

2011

dbSNP: rs2736100
rs2736100
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung
C 0.800 GeneticVariation GWASCAT The combined analyses identified six well-replicated SNPs with independent effects and significant lung cancer associations (P < 5.0 × 10(-8)) located in TP63 (rs4488809 at 3q28, P = 7.2 × 10(-26)), TERT-CLPTM1L (rs465498 and rs2736100 at 5p15.33, P = 1.2 × 10(-20) and P = 1.0 × 10(-27), respectively), MIPEP-TNFRSF19 (rs753955 at 13q12.12, P = 1.5 × 10(-12)) and MTMR3-HORMAD2-LIF (rs17728461 and rs36600 at 22q12.2, P = 1.1 × 10(-11) and P = 6.2 × 10(-13), respectively). 21725308

2011

dbSNP: rs2736100
rs2736100
CUI: C0085136
Disease: Central Nervous System Neoplasms
Central Nervous System Neoplasms
0.800 GeneticVariation GWASCAT Chromosome 7p11.2 (EGFR) variation influences glioma risk. 21531791

2011

dbSNP: rs2736100
rs2736100
CUI: C0085136
Disease: Central Nervous System Neoplasms
Central Nervous System Neoplasms
G 0.800 GeneticVariation GWASCAT Genome-wide association study identifies five susceptibility loci for glioma. 19578367

2009

dbSNP: rs2736100
rs2736100
CUI: C0032181
Disease: Platelet Count measurement
Platelet Count measurement
0.700 GeneticVariation GWASCAT Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. 29403010

2018

dbSNP: rs2736100
rs2736100
Finding of Mean Corpuscular Hemoglobin
0.700 GeneticVariation GWASCAT Genome-wide Trans-ethnic Meta-analysis Identifies Seven Genetic Loci Influencing Erythrocyte Traits and a Role for RBPMS in Erythropoiesis. 28017375

2017

dbSNP: rs2736100
rs2736100
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result)
0.700 GeneticVariation GWASCAT Genome-wide Trans-ethnic Meta-analysis Identifies Seven Genetic Loci Influencing Erythrocyte Traits and a Role for RBPMS in Erythropoiesis. 28017375

2017

dbSNP: rs2736100
rs2736100
CUI: C0032181
Disease: Platelet Count measurement
Platelet Count measurement
A 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252

2016