Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Glioma
CUI: C0017638
Disease: Glioma
0.820 GeneticVariation GWASCAT Sex-specific glioma genome-wide association study identifies new risk locus at 3p21.31 in females, and finds sex-differences in risk at 8q24.21. 29743610 2018
Glioma
CUI: C0017638
Disease: Glioma
0.820 GeneticVariation GWASCAT Genome-wide association study of glioma subtypes identifies specific differences in genetic susceptibility to glioblastoma and non-glioblastoma tumors. 28346443 2017
Glioma
CUI: C0017638
Disease: Glioma
0.820 GeneticVariation BEFREE This meta-analysis demonstrates that the RTEL1 rs2297440 polymorphism plays a moderate, but significant role in the risk of gli</span>oma. 26939676 2016
Glioma
CUI: C0017638
Disease: Glioma
0.820 GeneticVariation BEFREE Two single variants, the genotypes of "GG" of rs6010620 and "CC" of rs2297440</span> (rs6010620 and rs2297440) in the RTEL1 gene, together with two haplotypes of GCT and ATT, were identified to be associated with glioma development. 23683922 2013
Glioma
CUI: C0017638
Disease: Glioma
0.820 GeneticVariation GWASDB Genome-wide association study identifies five susceptibility loci for glioma. 19578367 2009
Glioblastoma
CUI: C0017636
Disease: Glioblastoma
0.730 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
Glioblastoma Multiforme
CUI: C1621958
Disease: Glioblastoma Multiforme
0.730 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
Glioblastoma Multiforme
CUI: C1621958
Disease: Glioblastoma Multiforme
0.730 GeneticVariation GWASCAT Genome-wide association study of glioma subtypes identifies specific differences in genetic susceptibility to glioblastoma and non-glioblastoma tumors. 28346443 2017
Glioblastoma
CUI: C0017636
Disease: Glioblastoma
0.730 GeneticVariation GWASCAT Genome-wide association study of glioma subtypes identifies specific differences in genetic susceptibility to glioblastoma and non-glioblastoma tumors. 28346443 2017
Glioblastoma Multiforme
CUI: C1621958
Disease: Glioblastoma Multiforme
0.730 GeneticVariation BEFREE Using the χ(2) test, we found that rs2297440 and rs6010620 in RTEL1 increased risk of GBM. 26156397 2015
Glioblastoma
CUI: C0017636
Disease: Glioblastoma
0.730 GeneticVariation BEFREE Using the χ(2) test, we found that rs2297440 and rs6010620 in RTEL1 increased risk of GBM. 26156397 2015
Glioblastoma
CUI: C0017636
Disease: Glioblastoma
0.730 GeneticVariation BEFREE The opposite is true of RTEL (20q13) region polymorphisms, which are significantly associated with glioblastoma (rs2297440, OR = 0.56, P = 4.6 × 10(-10)) but not oligodendroglial tumor. 21356187 2011
Glioblastoma Multiforme
CUI: C1621958
Disease: Glioblastoma Multiforme
0.730 GeneticVariation BEFREE The opposite is true of RTEL (20q13) region polymorphisms, which are significantly associated with glioblastoma (rs2297440, OR = 0.56, P = 4.6 × 10(-10)) but not oligodendroglial tumor. 21356187 2011
Glioblastoma
CUI: C0017636
Disease: Glioblastoma
0.730 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
Glioblastoma Multiforme
CUI: C1621958
Disease: Glioblastoma Multiforme
0.730 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
Central Nervous System Neoplasms
CUI: C0085136
Disease: Central Nervous System Neoplasms
0.700 GeneticVariation GWASCAT Genome-wide association study of glioma subtypes identifies specific differences in genetic susceptibility to glioblastoma and non-glioblastoma tumors. 28346443 2017
Astrocytoma
CUI: C0004114
Disease: Astrocytoma
0.020 GeneticVariation BEFREE Moreover, the stratified analyses showed a decreased risk of astrocytoma associated with RTEL1 rs6089953, rs6010620 and rs2297440 (p trend = 0.022, p trend = 0.042, p trend = 0.029, respectively) as well as an increased risk of this subtype associated with RTEL1 rs4809324 (p trend = 0.033). 26014354 2015
Childhood Astrocytoma
CUI: C4086152
Disease: Childhood Astrocytoma
0.020 GeneticVariation BEFREE Moreover, the stratified analyses showed a decreased risk of astrocytoma associated with RTEL1 rs6089953, rs6010620 and rs2297440 (p trend = 0.022, p trend = 0.042, p trend = 0.029, respectively) as well as an increased risk of this subtype associated with RTEL1 rs4809324 (p trend = 0.033). 26014354 2015
Astrocytoma
CUI: C0004114
Disease: Astrocytoma
0.020 GeneticVariation BEFREE In the recessive model, we found two tSNPs (rs2297440 and rs6010620) associated with increased astrocytoma risk. 23812731 2013
Childhood Astrocytoma
CUI: C4086152
Disease: Childhood Astrocytoma
0.020 GeneticVariation BEFREE In the recessive model, we found two tSNPs (rs2297440 and rs6010620) associated with increased astrocytoma risk. 23812731 2013
Oligodendroglial Neoplasm
CUI: C1335110
Disease: Oligodendroglial Neoplasm
0.010 GeneticVariation BEFREE The opposite is true of RTEL (20q13) region polymorphisms, which are significantly associated with glioblastoma (rs2297440, OR = 0.56, P = 4.6 × 10(-10)) but not oligodendroglial tumor. 21356187 2011
Childhood Glioblastoma
CUI: C0280474
Disease: Childhood Glioblastoma
0.010 GeneticVariation BEFREE The opposite is true of RTEL (20q13) region polymorphisms, which are significantly associated with glioblastoma (rs2297440, OR = 0.56, P = 4.6 × 10(-10)) but not oligodendroglial tumor. 21356187 2011
Adult Oligodendroglial Tumor
CUI: C1541567
Disease: Adult Oligodendroglial Tumor
0.010 GeneticVariation BEFREE The opposite is true of RTEL (20q13) region polymorphisms, which are significantly associated with glioblastoma (rs2297440, OR = 0.56, P = 4.6 × 10(-10)) but not oligodendroglial tumor. 21356187 2011
Adult Glioblastoma
CUI: C0278878
Disease: Adult Glioblastoma
0.010 GeneticVariation BEFREE The opposite is true of RTEL (20q13) region polymorphisms, which are significantly associated with glioblastoma (rs2297440, OR = 0.56, P = 4.6 × 10(-10)) but not oligodendroglial tumor. 21356187 2011