Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs104894103
rs104894103
0.010 GeneticVariation BEFREE CoQ10 deficiency has been identified in fibroblasts and muscle of AOA1 patients carrying the common W279X mutation, and aprataxin has been localized to mitochondria in neuroblastoma cells, where it enhances preservation of mitochondrial function. 25976310

2015

dbSNP: rs1051266
rs1051266
0.010 GeneticVariation BEFREE The aim of this study was to investigate the association between MTHFR rs1801133 (C677T) and RFC-1 rs1051266 (G80A) genotypes with the risk of developing nephroblastoma and neuroblastoma. 25536437

2015

dbSNP: rs1052133
rs1052133
0.010 GeneticVariation BEFREE Stratified analysis revealed that rs1052133</span> GC/CC carriers were less likely to develop neuroblastoma in subgroups of age >18 months, males, tumor that develops from retroperitoneal, mediastinum and clinical stage I+II+4s. 30519358

2018

dbSNP: rs1052536
rs1052536
0.010 GeneticVariation BEFREE These results suggest that rs1052536 C>T and rs4796030 A>C are unrelated to neuroblastoma susceptibility in the Chinese population. 31737108

2019

dbSNP: rs1057519697
rs1057519697
ALK
0.010 GeneticVariation BEFREE We detected the ALK mutation (F1174C and R1275Q) in 2 (3.7%) of the 54 NB specimens. 21940108

2011

dbSNP: rs1057520018
rs1057520018
0.010 GeneticVariation BEFREE A heterozygous missense mutation in STK11 (F354L) was identified in both the NB and FVPTC. 25751324

2015

dbSNP: rs1059111
rs1059111
0.010 GeneticVariation BEFREE The neurofilament gene NEFL harbored three SNPs associated with neuroblastoma (rs11994014: Pcombined = 0.0050; OR, 0.88; rs2979704: Pcombined = 0.0072; OR, 0.87; rs1059111: Pcombined = 0.0049; OR, 0.86). 25312269

2014

dbSNP: rs10840002
rs10840002
0.040 GeneticVariation BEFREE <b>Objective:</b> We conducted a three-center case-control study including 313 cases and 716 controls with the purpose to evaluate the association between five GWAS-identified <i>LMO1</i> variants (rs110419 A>G, rs4758051 G>A, rs10840002 A>G, rs204938 A>G, and rs2168101 G>T) and neuroblastoma susceptibility in eastern Chinese children. 30406033

2018

dbSNP: rs10840002
rs10840002
0.040 GeneticVariation BEFREE In addition, the rs4758051 variant appeared protective against NB in homozygous, dominant and allele genetic models, whereas the rs10840002 variant markedly decreased the risk of NB in the allele model. 31830377

2020

dbSNP: rs10840002
rs10840002
0.040 GeneticVariation BEFREE In a combination analysis using Southern and Northern Chinese populations, we found that those carrying the rs110419 G, rs4758051 A or rs10840002 G allele were at decreased neuroblastoma risk, and this finding was supported by a false-positive report probability analysis. 29029458

2017

dbSNP: rs10840002
rs10840002
0.040 GeneticVariation BEFREE Previous genome-wide association study (GWAS) indicated that several common genetic variations (rs110419 A > G, rs4758051 G > A, rs10840002 A > G and rs204938 A > G) in the LIM domain only 1 (LMO1) gene were associated with neuroblastoma susceptibility. 27009839

2016

dbSNP: rs10895322
rs10895322
0.010 GeneticVariation BEFREE Here we identify common variants at 11q22.2 within MMP20 that associate with neuroblastoma cases harboring 11q deletion (rs10895322), using GWAS in 113 European-American cases and 5109 ancestry-matched controls. 28924153

2017

dbSNP: rs11037575
rs11037575
0.010 GeneticVariation BEFREE In conclusion, we verified that the <i>HSD17B12</i> rs11037575 T allele might negatively associate with neuroblastoma risk. 28435286

2017

dbSNP: rs110419
rs110419
0.050 GeneticVariation BEFREE Our findings revealed that rs110419 and rs2168101 polymorphisms were significantly associated with a decreased risk of NB in all genetic models. 31830377

2020

dbSNP: rs110419
rs110419
0.050 GeneticVariation BEFREE We found that the rs110419 A > G polymorphism was associated with a significantly decreased neuroblastoma</span> risk (AG vs. AA: adjusted OR = 0.65, 95% CI = 0.47-0.91; GG vs. AA: adjusted OR = 0.58, 95% CI = 0.36-0.91; AG/GG vs. AA: adjusted OR = 0.63, 95% CI = 0.46-0.86), and the protective effect was more predominant in children of age > 18 months, males, subgroups with tumor in adrenal gland and mediastinum, and patients in clinical stages III/IV. 27009839

2016

dbSNP: rs110419
rs110419
0.050 GeneticVariation BEFREE <b>Results:</b> Significant associations with neuroblastoma risk were found for four (rs110419, rs4758051, rs10840002, and rs2168101) out of the five polymorphisms. 30406033

2018

dbSNP: rs110419
rs110419
0.050 GeneticVariation BEFREE We also confirmed that rs6939340 A>G (G versus A: OR=1.30, 95% CI=1.13-1.50) and rs110419 G>A (A versus G: OR=1.37, 95% CI=1.19-1.58) were associated with increased neur</span>oblastoma risk for all subjects. 29024823

2017

dbSNP: rs110419
rs110419
0.050 GeneticVariation BEFREE A major haplotype, ATC, containing rs204926, rs110420, and rs110419, conferred a significant increase in risk for NB (OR = 1.82, 95% CI: 1.41-2.36, adjusted P < 0.001). 26030754

2015

dbSNP: rs110420
rs110420
0.010 GeneticVariation BEFREE A major haplotype, ATC, containing rs204926, rs110420, and rs110419, conferred a significant increase in risk for NB (OR = 1.82, 95% CI: 1.41-2.36, adjusted P < 0.001). 26030754

2015

dbSNP: rs11103603
rs11103603
0.010 GeneticVariation BEFREE Maternal rs6776706 was associated with (RR: 0.49; 95% CI: 0.33-0.72, Q = 0.161) high-risk neuroblastoma and maternal rs11103603 (RR: 0.60; 95% CI: 0.45-0.79, Q = 0.127) was associated with neuroblastoma aged <1 year. 31279991

2019

dbSNP: rs11134527
rs11134527
0.010 GeneticVariation BEFREE Overall, the miR-34b/c rs4938723 T > C and miR-218 rs11134527 A > G polymorphisms displayed a protective role from neuroblastoma.These findings need further validation. 29858046

2018

dbSNP: rs11247957
rs11247957
0.010 GeneticVariation BEFREE Herein, we evaluated the correlation of four potentially functional LIN28A SNPs (rs3811464 G>A, rs3811463 T>C, rs34787247 G>A, and rs11247957 G>A) and neuroblastoma susceptibility in 505 neuroblastoma patients and 1070 controls from four independent hospitals in China. 31747721

2020

dbSNP: rs1130409
rs1130409
0.010 GeneticVariation BEFREE Here, we conducted a three-center case-control study to evaluate the association between <i>APEX1</i> polymorphisms (rs1130409 T>G, rs1760944 T>G, and rs3136817 T>C) and neuroblastoma risk in Chinese children, consisting of 469 cases and 998 controls. 31341530

2019

dbSNP: rs1131691014
rs1131691014
0.010 GeneticVariation BEFREE Overall, we confirmed that miR-34b/c rs4938723 and TP53 Arg72Pro conferred decreased neuroblastoma risk and two polymorphisms exerted stronger protective effects against neuroblastoma than either one alone. 31325764

2019

dbSNP: rs113488022
rs113488022
0.010 GeneticVariation BEFREE To explore the mutation frequencies of BRAF(V600E) (V-raf murine sarcoma virus oncogene homolog B1) and NRAS (neuroblastoma ras viral oncogene homolog) codon 61 in CMNs of Chinese, we selected 55 paraffin-embedded tissue blocks, including 37 cases of medium CMNs (1.5-20cm) and 18 cases of giant CMNs (>20 cm). 21430505

2011