Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs110419
rs110419
0.850 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
0.850 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
0.850 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
0.850 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
0.850 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: rs110419
rs110419
A 0.850 GeneticVariation GWASDB Common variation at 6q16 within HACE1 and LIN28B influences susceptibility to neuroblastoma. 22941191

2012

dbSNP: rs110419
rs110419
A 0.850 GeneticVariation GWASCAT Common variation at 6q16 within HACE1 and LIN28B influences susceptibility to neuroblastoma. 22941191

2012

dbSNP: rs110419
rs110419
A 0.850 GeneticVariation GWASCAT Integrative genomics identifies LMO1 as a neuroblastoma oncogene. 21124317

2011

dbSNP: rs110419
rs110419
A 0.850 GeneticVariation GWASDB Integrative genomics identifies LMO1 as a neuroblastoma oncogene. 21124317

2011

dbSNP: rs2168101
rs2168101
0.730 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: rs2168101
rs2168101
0.730 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: rs2168101
rs2168101
0.730 GeneticVariation BEFREE In summary, the current study confirmed that the potentially functional <i>LMO1</i> rs2168101 G>T and rs3750952 G>C polymorphisms were associated with neuroblastoma susceptibility. 29760797

2018

dbSNP: rs2168101
rs2168101
C 0.730 GeneticVariation GWASCAT Common variants upstream of MLF1 at 3q25 and within CPZ at 4p16 associated with neuroblastoma. 28545128

2017

dbSNP: rs204938
rs204938
0.040 GeneticVariation BEFREE In contrast, the rs204938 polymorphism showed a positive association with NB susceptibility in allele genetic models. 31830377

2020

dbSNP: rs204938
rs204938
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: rs204938
rs204938
0.040 GeneticVariation BEFREE In this work, we used Taqman methodology to genotype four <i>LMO1</i> polymorphisms (rs110419 A > G, rs4758051 G > A, rs10840002 A > G and rs204938 A > G) in 118 neuroblastoma cases and 281 controls from Northern China. 29029458

2017

dbSNP: rs204938
rs204938
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: rs3750952
rs3750952
0.010 GeneticVariation BEFREE In summary, the current study confirmed that the potentially functional <i>LMO1</i> rs2168101 G>T and rs3750952 G>C polymorphisms were associated with neuroblastoma susceptibility. 29760797

2018

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: rs204926
rs204926
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