Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121913400
rs121913400
0.810 GeneticVariation BEFREE These mutations caused amino acid substitutions in 3 of 80 medulloblastomas (Ser33Phe, Ser33Cys and Ser37Cys) and 1 of 4 supratentorial PNETs (Gly34Val). 11433413

2001

dbSNP: rs1042522
rs1042522
0.020 GeneticVariation BEFREE With regard to prognosis, disease-free survival was not significantly different among the TP53 Arg72Pro SNP</span> genotypes (P > 0.05), but the less frequent genotype (Pro/Pro) was associated with shorter overall survival of medulloblastoma patients (P = 0.021). 22886512

2012

dbSNP: rs1042522
rs1042522
0.020 GeneticVariation BEFREE Loss of heterozygosity and p53 polymorphism Pro72Arg in a young patient with medulloblastoma. 12684657

2003

dbSNP: rs1131691014
rs1131691014
0.020 GeneticVariation BEFREE With regard to prognosis, disease-free survival was not significantly different among the TP53 Arg72Pro SNP</span> genotypes (P > 0.05), but the less frequent genotype (Pro/Pro) was associated with shorter overall survival of medulloblastoma patients (P = 0.021). 22886512

2012

dbSNP: rs1131691014
rs1131691014
0.020 GeneticVariation BEFREE Loss of heterozygosity and p53 polymorphism Pro72Arg in a young patient with medulloblastoma. 12684657

2003

dbSNP: rs61754966
rs61754966
NBN
0.020 GeneticVariation BEFREE Our results indicate that heterozygous carriers of the germ-line NBN gene mutations (c.511A>G and c.657_661del5) may exhibit increased susceptibility to developing MB. 19908051

2010

dbSNP: rs61754966
rs61754966
NBN
0.020 GeneticVariation BEFREE Among children with solid tumors only in 1 child with medulloblastoma I171V variant has been found. 21436738

2011

dbSNP: rs878854066
rs878854066
0.020 GeneticVariation BEFREE Loss of heterozygosity and p53 polymorphism Pro72Arg in a young patient with medulloblastoma. 12684657

2003

dbSNP: rs878854066
rs878854066
0.020 GeneticVariation BEFREE With regard to prognosis, disease-free survival was not significantly different among the TP53 Arg72Pro SNP</span> genotypes (P > 0.05), but the less frequent genotype (Pro/Pro) was associated with shorter overall survival of medulloblastoma patients (P = 0.021). 22886512

2012

dbSNP: rs1051740
rs1051740
0.010 GeneticVariation BEFREE However, the maternal EPHX1 rs1051740 genotype (RR = 3.26, P = .01) was associated with medulloblastoma risk. 22994552

2012

dbSNP: rs1057517558
rs1057517558
APC
0.010 GeneticVariation BEFREE The medulloblastoma cell line MHH-MED-2 carried a Glu1317Gln missense germline variant and a sporadic MB sample showed a somatic Pro1319Leu substitution. 11433413

2001

dbSNP: rs1063192
rs1063192
0.010 GeneticVariation BEFREE We hypothesized that CCDKN2A/B rs1063192 and rs4977756 and also the long noncoding RNA (lncRNA) CDKN2BAS rs2157719 glioma susceptibility polymorphisms identified by genome-wide association studies may contribute to medulloblastoma predisposition. 29314442

2018

dbSNP: rs113488022
rs113488022
0.010 GeneticVariation BEFREE The ability of the polio: rhinovirus recombinant, PVSRIPO, to infect PXA (645 [BRAF V600E mutation], 2363) and medulloblastoma (D283, D341) cells were determined by viral propagation measurement and cell proliferation. 29878245

2018

dbSNP: rs121913377
rs121913377
0.010 GeneticVariation BEFREE The ability of the polio: rhinovirus recombinant, PVSRIPO, to infect PXA (645 [BRAF V600E mutation], 2363) and medulloblastoma (D283, D341) cells were determined by viral propagation measurement and cell proliferation. 29878245

2018

dbSNP: rs121918457
rs121918457
0.010 GeneticVariation BEFREE We present a patient with NSML caused by the recurrent PTPN11 mutation c.1403C > T (p.Thr468Met) in whom medulloblastoma was diagnosed at age 10 years. 23813970

2013

dbSNP: rs13306747
rs13306747
0.010 GeneticVariation BEFREE Of the eight SNPs identified, PPARα (rs6008197), PPARγ (rs13306747), and PPARδ (rs3734254) were most significantly associated with long-term changes in general intellectual functioning in medulloblastoma survivors. 30607709

2019

dbSNP: rs1333957805
rs1333957805
0.010 GeneticVariation BEFREE In a series of 90 MBs and 8 MB cell lines, we found one germline and one somatic mutation resulting in amino acid substitutions in the first (Ile53Leu) and second (Asp97Asn) transmembrane regions, respectively. 15880586

2005

dbSNP: rs139209450
rs139209450
0.010 GeneticVariation BEFREE In 2 further MB biopsies, mutations were identified in exon 5 (Glu408Lys) and exon 8 (Ser738Phe) of the AXIN2 gene, which are due to predicted germline mutations and rare polymorphisms. mRNA expression analysis in 22 MBs revealed reduced expression of AXIN2 mRNA compared to 8 fetal cerebellar tissues. 17373666

2007

dbSNP: rs1400239417
rs1400239417
ALK
0.010 GeneticVariation BEFREE Identification of a novel inherited ALK variant M1199L in the WNT type of medulloblastoma. 27179218

2016

dbSNP: rs143277125
rs143277125
0.010 GeneticVariation BEFREE We report the case of a 16-year-old female with duodenal adenocarcinoma and past history of medulloblastoma found to have a novel germline bialleleic truncating mutation (c.[949C>T]+[949C>T]) of the PMS2 gene. 19283792

2009

dbSNP: rs144848
rs144848
0.010 GeneticVariation BEFREE An Asn372His homozygous variation was noted in the BRCA2 gene in the patient with medulloblastoma whereas the variation was heterozygous in the healthy father. 22044372

2011

dbSNP: rs1801166
rs1801166
APC
0.010 GeneticVariation BEFREE The medulloblastoma cell line MHH-MED-2 carried a Glu1317Gln missense germline variant and a sporadic MB sample showed a somatic Pro1319Leu substitution. 11433413

2001

dbSNP: rs1801516
rs1801516
ATM
0.010 GeneticVariation BEFREE The polymorphism D1853N was reported in healthy individuals and medulloblastomas. 18465141

2008

dbSNP: rs2157719
rs2157719
0.010 GeneticVariation BEFREE Moreover, the association between the CDKN2BAS r</span>s2157719 polymorphism and medulloblastoma risk is more pronounced in males (OR = 2.22, 95% CI = 1.36-3.62; p = 0.001). 29314442

2018

dbSNP: rs3734254
rs3734254
0.010 GeneticVariation BEFREE Of the eight SNPs identified, PPARα (rs6008197), PPARγ (rs13306747), and PPARδ (rs3734254) were most significantly associated with long-term changes in general intellectual functioning in medulloblastoma survivors. 30607709

2019