Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
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: rs2273267
rs2273267
0.010 GeneticVariation BEFREE Further independent case-control studies with functional analysis are needed to verify the role of NRAS gene rs2273267 A>T polymorphism in the risk of neuroblastoma. 31759987

2020

dbSNP: rs34787247
rs34787247
0.010 GeneticVariation BEFREE Overall, our finding indicated that LIN28A SNPs, especially rs34787247 G>A, may increase neuroblastoma risk. 31747721

2020

dbSNP: rs3811463
rs3811463
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: rs3811464
rs3811464
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: rs1024611
rs1024611
0.010 GeneticVariation BEFREE Dual-luciferase reporter assays were conducted in neuroblastoma cells to assess the promoter transcriptional activity of the rs1024611 variants (T>C) and the GRCh38.p12chr17:34252593 G>C alleles in CCL2. 30761072

2019

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: 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: 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: rs121909536
rs121909536
0.010 GeneticVariation BEFREE We generated SH-SY5Y neuroblastoma cell lines constitutively expressing wild type (WT) Hemagglutinin (HA) epitope tagged mouse Ang1 (mAng1), and two amyotrophic lateral sclerosis associated ANG variants (C39W and K40I). 31128105

2019

dbSNP: rs121909539
rs121909539
0.010 GeneticVariation BEFREE We generated SH-SY5Y neuroblastoma cell lines constitutively expressing wild type (WT) Hemagglutinin (HA) epitope tagged mouse Ang1 (mAng1), and two amyotrophic lateral sclerosis associated ANG variants (C39W and K40I). 31128105

2019

dbSNP: rs12442054
rs12442054
0.010 GeneticVariation BEFREE One maternal SNP (rs12442054) was associated with decreased risk of neuroblastoma (RR: 0.61; 95% Confidence Interval (CI): 0.47-0.79, Q = 0.076). 31279991

2019

dbSNP: rs12587
rs12587
0.010 GeneticVariation BEFREE We conducted a four-center case-control study to explore the association between <i>KRAS</i> gene polymorphisms (rs12587 G>T, rs7973450 A>G, rs7312175 G>A) and neuroblastoma susceptibility with 505 Chinese children and 1070 matched controls. 31564912

2019

dbSNP: rs1362575880
rs1362575880
0.010 GeneticVariation BEFREE The effects of these two mutations on presenilin-1 endoproteolysis and β-amyloid (Aβ) production were examined in SH-SY5Y neuroblastoma cells infected with lentiviruses expressing presenilin-1 wild type (WT), I249L and P433S mutants. 31235249

2019

dbSNP: rs17487792
rs17487792
0.010 GeneticVariation BEFREE After adjusted gender and age, seven out of eleven SNPs in <i>BARD1</i> were significant associated with the risk of NB, including one SNP in 5'-UTR (rs17489363 G > A), two SNPs in exon (rs2229571 G > C and rs3738888 C > T), and four SNPs in intron (rs3768716 A > G, rs6435862 T > G, rs3768707 C > T and rs17487792 C > T). 31258718

2019

dbSNP: rs1760944
rs1760944
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: rs2153977
rs2153977
0.010 GeneticVariation BEFREE In vitro and in silico analyses indicated that the rs2153977-T protective allele, located in an NB and CMM enhancer, decreased expression of SLC16A1 via long-range loop formation and altered a T-box protein binding site. 31605138

2019

dbSNP: rs28933981
rs28933981
TTR
0.010 GeneticVariation BEFREE Cytotoxicity assays revealed their toxicities in the order of Val30Met > Ala97Ser > WT > Thr119Met in neuroblastoma cells. 31728576

2019

dbSNP: rs3136817
rs3136817
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: rs3738888
rs3738888
0.010 GeneticVariation BEFREE After adjusted gender and age, seven out of eleven SNPs in <i>BARD1</i> were significant associated with the risk of NB, including one SNP in 5'-UTR (rs17489363 G > A), two SNPs in exon (rs2229571 G > C and rs3738888 C > T), and four SNPs in intron (rs3768716 A > G, rs6435862 T > G, rs3768707 C > T and rs17487792 C > T). 31258718

2019

dbSNP: rs3768707
rs3768707
0.010 GeneticVariation BEFREE After adjusted gender and age, seven out of eleven SNPs in <i>BARD1</i> were significant associated with the risk of NB, including one SNP in 5'-UTR (rs17489363 G > A), two SNPs in exon (rs2229571 G > C and rs3738888 C > T), and four SNPs in intron (rs3768716 A > G, rs6435862 T > G, rs3768707 C > T and rs17487792 C > T). 31258718

2019

dbSNP: rs4796030
rs4796030
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: rs6776706
rs6776706
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: rs729147
rs729147
0.010 GeneticVariation BEFREE For gene-environment interaction, maternal rs729147 was associated with decreased risk of neuroblastoma among mothers with vitamin A consumption above the recommendation. 31279991

2019