Gene: RTEL1 ×
Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs6010620
rs6010620
RTEL1 ; RTEL1-TNFRSF6B
0.900 GeneticVariation BEFREE 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: rs6010620
rs6010620
RTEL1 ; RTEL1-TNFRSF6B
G 0.900 GeneticVariation GWASDB 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: rs2297440
rs2297440
RTEL1 ; RTEL1-TNFRSF6B
C 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
dbSNP: rs2297440
rs2297440
RTEL1 ; RTEL1-TNFRSF6B
C 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
dbSNP: rs2297440
rs2297440
RTEL1 ; RTEL1-TNFRSF6B
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
dbSNP: rs2297440
rs2297440
RTEL1 ; RTEL1-TNFRSF6B
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
dbSNP: rs2297440
rs2297440
RTEL1 ; RTEL1-TNFRSF6B
0.820 GeneticVariation GWASDB Genome-wide association study identifies five susceptibility loci for glioma. 19578367

2009
dbSNP: rs4809324
rs4809324
RTEL1 ; RTEL1-TNFRSF6B
C 0.800 GeneticVariation GWASDB Variants in the CDKN2B and RTEL1 regions are associated with high-grade glioma susceptibility. 19578366

2009
dbSNP: rs4809324
rs4809324
RTEL1 ; RTEL1-TNFRSF6B
C 0.800 GeneticVariation GWASCAT Variants in the CDKN2B and RTEL1 regions are associated with high-grade glioma susceptibility. 19578366

2009
dbSNP: rs2236507
rs2236507
RTEL1 ; RTEL1-TNFRSF6B
C 0.700 GeneticVariation GWASCAT Genome-wide association study identifies multiple susceptibility loci for glioma. 26424050

2015
dbSNP: rs115303435
rs115303435
TNFRSF6B ; RTEL1 ; RTEL1-TNFRSF6B
0.010 GeneticVariation BEFREE The glioma subgroup analyses showed that the causal variants (rs6062302 and rs115303435) may be associated with increased risk of glioma</span> regardless of histological grades and molecular alterations. 30462709

2018
dbSNP: rs6062302
rs6062302
RTEL1 ; RTEL1-TNFRSF6B
0.010 GeneticVariation BEFREE The glioma subgroup analyses showed that the causal variants (rs6062302 and rs115303435) may be associated with increased risk of glioma regardless of histological grades and molecular alterations. 30462709

2018