Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1582417
rs1582417
0.010 GeneticVariation BEFREE Our study provided the first evidence for the impact of rs1582417, rs17057846, rs2431689, rs2961920, rs58747524, and rs7727115 polymorphisms in MIR3142HG on the susceptibility to and/or prognosis of glioma in the Chinese Han population. 31513017

2020

dbSNP: rs17057846
rs17057846
0.010 GeneticVariation BEFREE In the risk analysis, rs17057846 (odds ratio [OR]=1.93, P=0.047), rs2961920 (OR=1.53, P=0.019), and rs58747524 (OR=1.23, P=0.046) polymorphisms were associated with increased glioma risk, while rs7727115 (OR=0.76, P=0.030) and rs1582417 (female individuals, OR=0.49, P=0.017) variants were associated with decreased risk. 31513017

2020

dbSNP: rs2961920
rs2961920
0.010 GeneticVariation BEFREE In the risk analysis, rs17057846 (odds ratio [OR]=1.93, P=0.047), rs2961920 (OR=1.53, P=0.019), and rs58747524 (OR=1.23, P=0.046) polymorphisms were associated with increased glioma risk, while rs7727115 (OR=0.76, P=0.030) and rs1582417 (female individuals, OR=0.49, P=0.017) variants were associated with decreased risk. 31513017

2020

dbSNP: rs58747524
rs58747524
0.010 GeneticVariation BEFREE Our study provided the first evidence for the impact of rs1582417, rs17057846, rs2431689, rs2961920, rs58747524, and rs7727115 polymorphisms in MIR3142HG on the susceptibility to and/or prognosis of glioma in the Chinese Han population. 31513017

2020

dbSNP: rs7727115
rs7727115
0.010 GeneticVariation BEFREE Our study provided the first evidence for the impact of rs1582417, rs17057846, rs2431689, rs2961920, rs58747524, and rs7727115 polymorphisms in MIR3142HG on the susceptibility to and/or prognosis of glioma in the Chinese Han population. 31513017

2020

dbSNP: rs1044129
rs1044129
0.010 GeneticVariation BEFREE This study evaluated the role of TYMS (rs1059394, C > T, and rs2847153, G > A), RYR3 (rs1044129, G > A), KIAA0423 (rs1053667, T > C), and GOLGA7 (rs11337, G > T) polymorphisms for assessment of glioma risk and prognosis among the Chinese Han population. 31525662

2019

dbSNP: rs1053667
rs1053667
0.010 GeneticVariation BEFREE This study evaluated the role of TYMS (rs1059394, C > T, and rs2847153, G > A), RYR3 (rs1044129, G > A), KIAA0423 (rs1053667, T > C), and GOLGA7 (rs11337, G > T) polymorphisms for assessment of glioma risk and prognosis among the Chinese Han population. 31525662

2019

dbSNP: rs1057519902
rs1057519902
0.010 GeneticVariation BEFREE We report the case of a 17-year-old female with an H3F3A G34R mutated infiltrative glioma who developed painful osseous metastases to her pelvis and spine within 3 months of clinical presentation. 31139567

2019

dbSNP: rs1131239
rs1131239
0.010 GeneticVariation BEFREE Haplotype analysis showed that haplotype ″GACCG″ in the block (rs41278075, rs2306420, rs117677079, rs2306415 and rs1131239) significantly decreased the susceptibility of glioma (OR 0.61, p = 0.003). 30536196

2019

dbSNP: rs11337
rs11337
0.010 GeneticVariation BEFREE These results suggest that GOLGA7 (rs11337) polymorphism may play a role in the prognosis of glioma patients and that TYMS (rs1059394) is associated with glioma risk. 31525662

2019

dbSNP: rs117677079
rs117677079
0.010 GeneticVariation BEFREE Haplotype analysis showed that haplotype ″GACCG″ in the block (rs41278075, rs2306420, rs117677079</span>, rs2306415 and rs1131239) significantly decreased the susceptibility of glioma (OR 0.61, p = 0.003). 30536196

2019

dbSNP: rs1339499
rs1339499
0.010 GeneticVariation BEFREE Furthermore, cumulative associations of rs473426 and rs1339499 with glioma risk were observed (P = 0.011). 31773361

2019

dbSNP: rs145619195
rs145619195
0.010 GeneticVariation BEFREE Whereas, rs145619195 CT genotype might weaken the susceptibility (OR 0.63, p = 0.024) and prognosis (HR 0.20, p = 0.025) of glioma. 30536196

2019

dbSNP: rs145929329
rs145929329
0.010 GeneticVariation BEFREE Three adult glioma risk variants, rs634537, rs2157719, and rs145929329, all mapping to the 9p21.3 (<i>CDKN2B-AS1</i>) locus, were associated with glioma risk in children and AYA. 31040135

2019

dbSNP: rs1553260624
rs1553260624
0.010 GeneticVariation BEFREE We report the case of a 17-year-old female with an H3F3A G34R mutated infiltrative glioma who developed painful osseous metastases to her pelvis and spine within 3 months of clinical presentation. 31139567

2019

dbSNP: rs2235544
rs2235544
0.010 GeneticVariation BEFREE The C-allele of the DI01 SNP rs2235544 was related to increased circulating free T3/ free T4 ratio in glioma and meningioma patients, indicating greater T4 to T3 conversion. 31452060

2019

dbSNP: rs2239647
rs2239647
0.010 GeneticVariation BEFREE Stratified analysis showed that rs2239647 increased the risk of glioma in female (OR = 1.62, p = 0.016). 31759389

2019

dbSNP: rs2279115
rs2279115
0.010 GeneticVariation BEFREE Stratification analyses by sex elucidated that BCL-2 rs2279115</span> was significantly associated with glioma</span> risk in males (OR = 0.41, 95% CI = 0.30-0.58, p = 1.0 × 10<sup>-7</sup>), but not in females (p > 0.05). 30481055

2019

dbSNP: rs2306415
rs2306415
0.010 GeneticVariation BEFREE Haplotype analysis showed that haplotype ″GACCG″ in the block (rs41278075, rs2306420, rs117677079, rs2306415 and rs1131239) significantly decreased the susceptibility of glioma (OR 0.61, p = 0.003). 30536196

2019

dbSNP: rs2306420
rs2306420
0.010 GeneticVariation BEFREE Haplotype analysis showed that haplotype ″GACCG″ in the block (rs41278075, rs2306420, rs117677079, rs2306415 and rs1131239) significantly decreased the susceptibility of glioma (OR 0.61, p = 0.003). 30536196

2019

dbSNP: rs3213801
rs3213801
0.010 GeneticVariation BEFREE Overall, our results indicated that POLK variants rs3213801 and rs5744533 are not associated with glioma risk and prognosis. 31595696

2019

dbSNP: rs34988193
rs34988193
0.010 GeneticVariation BEFREE IMPLICATIONS: This is the first study presenting an approach to screening many germline variants to identify variants predictive of survival and our application of this methodology revealed the germline variants rs61757955 and rs34988193 as being predictive of survival in patients with lower grade glioma. 30651372

2019

dbSNP: rs3787016
rs3787016
0.010 GeneticVariation BEFREE Impact of four lncRNA polymorphisms (rs2151280, rs7763881, rs1136410, and rs3787016) on glioma risk and prognosis: A case-control study. 31489712

2019

dbSNP: rs41278075
rs41278075
0.010 GeneticVariation BEFREE Haplotype analysis showed that haplotype ″GACCG″ in the block (rs41278075, rs2306420, rs117677079, rs2306415 and rs1131239) significantly decreased the susceptibility of glioma (OR 0.61, p = 0.003). 30536196

2019

dbSNP: rs4598633
rs4598633
0.010 GeneticVariation BEFREE Rs7115578 polymorphism had a lower susceptibility to glioma in males (OR = 0.68, P=0.034), while rs4598633 variant with a higher risk in females (OR = 1.66, P=0.016). 31652449

2019