Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs224278
rs224278
C 0.800 GeneticVariation GWASDB Common variants near TARDBP and EGR2 are associated with susceptibility to Ewing sarcoma. 22327514

2012

dbSNP: rs224278
rs224278
C 0.800 GeneticVariation GWASCAT Common variants near TARDBP and EGR2 are associated with susceptibility to Ewing sarcoma. 22327514

2012

dbSNP: rs4924410
rs4924410
A 0.800 GeneticVariation GWASDB Common variants near TARDBP and EGR2 are associated with susceptibility to Ewing sarcoma. 22327514

2012

dbSNP: rs4924410
rs4924410
A 0.800 GeneticVariation GWASCAT Common variants near TARDBP and EGR2 are associated with susceptibility to Ewing sarcoma. 22327514

2012

dbSNP: rs9430161
rs9430161
G 0.800 GeneticVariation GWASCAT Common variants near TARDBP and EGR2 are associated with susceptibility to Ewing sarcoma. 22327514

2012

dbSNP: rs9430161
rs9430161
G 0.800 GeneticVariation GWASDB Common variants near TARDBP and EGR2 are associated with susceptibility to Ewing sarcoma. 22327514

2012

dbSNP: rs12106193
rs12106193
C 0.700 GeneticVariation GWASCAT Genome-wide association study identifies multiple new loci associated with Ewing sarcoma susceptibility. 30093639

2018

dbSNP: rs6106336
rs6106336
G 0.700 GeneticVariation GWASCAT Genome-wide association study identifies multiple new loci associated with Ewing sarcoma susceptibility. 30093639

2018

dbSNP: rs7744366
rs7744366
G 0.700 GeneticVariation GWASCAT Genome-wide association study identifies multiple new loci associated with Ewing sarcoma susceptibility. 30093639

2018

dbSNP: rs7832583
rs7832583
T 0.700 GeneticVariation GWASCAT Genome-wide association study identifies multiple new loci associated with Ewing sarcoma susceptibility. 30093639

2018

dbSNP: rs11576658
rs11576658
0.700 GeneticVariation GWASDB Common variants near TARDBP and EGR2 are associated with susceptibility to Ewing sarcoma. 22327514

2012

dbSNP: rs2003046
rs2003046
0.700 GeneticVariation GWASDB Common variants near TARDBP and EGR2 are associated with susceptibility to Ewing sarcoma. 22327514

2012

dbSNP: rs8026641
rs8026641
0.700 GeneticVariation GWASDB Common variants near TARDBP and EGR2 are associated with susceptibility to Ewing sarcoma. 22327514

2012

dbSNP: rs944684
rs944684
0.700 GeneticVariation GWASDB Common variants near TARDBP and EGR2 are associated with susceptibility to Ewing sarcoma. 22327514

2012

dbSNP: rs752536342
rs752536342
T 0.700 GeneticVariation CLINVAR

dbSNP: rs772295894
rs772295894
NF1
A 0.700 CausalMutation CLINVAR

dbSNP: rs231775
rs231775
0.020 GeneticVariation BEFREE Here, we investigated the association of four CTLA-4 gene polymorphisms, -1661A/G (rs4553808), -318C/T (rs5742909), +49G/A (rs231775), and CT60A/G (rs3087243), with ES in the Chinese population. 23480667

2013

dbSNP: rs5742909
rs5742909
0.020 GeneticVariation BEFREE Here, we investigated the association of four CTLA-4 gene polymorphisms, -1661A/G (rs4553808), -318C/T (rs5742909), +49G/A (rs231775), and CT60A/G (rs3087243), with ES in the Chinese population. 23480667

2013

dbSNP: rs231775
rs231775
0.020 GeneticVariation BEFREE The current study evaluated the association of two CTLA-4 gene polymorphisms, -318C/T (rs5742909) and +49G/A (rs231775) with ES in the Chinese population. 22905924

2012

dbSNP: rs5742909
rs5742909
0.020 GeneticVariation BEFREE The current study evaluated the association of two CTLA-4 gene polymorphisms, -318C/T (rs5742909) and +49G/A (rs231775) with ES in the Chinese population. 22905924

2012

dbSNP: rs1042522
rs1042522
0.010 GeneticVariation BEFREE In the present meta-analysis, we aimed to elucidate the associations of TP53 rs1042522 genetic polymorphism with the risk of osteosarcoma or Ewing sarcoma. 30833364

2019

dbSNP: rs11188147
rs11188147
0.010 GeneticVariation BEFREE We also replicated associations with rs4148737 in the ATP-binding cassette subfamily B member 1 (ABCB1) gene (discovery: HR = 2.96, 95% CI = 1.08-8.10, P = 0.034; replication: HR = 1.60, 95% CI = 1.05-2.44, P = 0.029), which we have previously found to be associated with poorer OS in pediatric osteosarcoma patients, and rs11188147 in cytochrome P450 family 2 subfamily C member 8 gene (CYP2C8) (discovery : HR = 2.49, 95% CI = 1.06-5.87, P = 0.037; replication: HR = 1.77, 95% CI = 1.06-2.96, P = 0.030), an enzyme involved in the oxidative metabolism of the ES chemotherapeutic agents cyclophosphamide and ifosfamide. 27287205

2016

dbSNP: rs311059
rs311059
0.010 GeneticVariation BEFREE The CD99 rs311059 T variant was found to be significantly associated [P value = 0.0029; ORhet = 3.9 (95% CI 1.5-9.8) and ORhom = 5.3 (95% CI 1.2-23.7)] with EWS onset in patients less than 14 years old, while the CD99 rs312257-T was observed to be associated [P value = 0.0265; ORhet = 3.5 (95% CI 1.3-9.9)] with a reduced risk of relapse. 27792997

2016

dbSNP: rs312257
rs312257
0.010 GeneticVariation BEFREE The CD99 rs311059 T variant was found to be significantly associated [P value = 0.0029; ORhet = 3.9 (95% CI 1.5-9.8) and ORhom = 5.3 (95% CI 1.2-23.7)] with EWS onset in patients less than 14 years old, while the CD99 rs312257-T was observed to be associated [P value = 0.0265; ORhet = 3.5 (95% CI 1.3-9.9)] with a reduced risk of relapse. 27792997

2016

dbSNP: rs4148737
rs4148737
0.010 GeneticVariation BEFREE We also replicated associations with rs4148737 in the ATP-binding cassette subfamily B member 1 (ABCB1) gene (discovery: HR = 2.96, 95% CI = 1.08-8.10, P = 0.034; replication: HR = 1.60, 95% CI = 1.05-2.44, P = 0.029), which we have previously found to be associated with poorer OS in pediatric osteosarcoma patients, and rs11188147 in cytochrome P450 family 2 subfamily C member 8 gene (CYP2C8) (discovery : HR = 2.49, 95% CI = 1.06-5.87, P = 0.037; replication: HR = 1.77, 95% CI = 1.06-2.96, P = 0.030), an enzyme involved in the oxidative metabolism of the ES chemotherapeutic agents cyclophosphamide and ifosfamide. 27287205

2016