Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121913666
rs121913666
Entrez Id: 4613
Gene Symbol: MYCN
MYCN
CUI: C4551774
Disease:
FEINGOLD SYNDROME 1
A 0.700 CausalMutation CLINVAR
dbSNP: rs121913667
rs121913667
Entrez Id: 4613;10408
Gene Symbol: MYCN;MYCNOS
MYCN;MYCNOS
CUI: C0796068
Disease:
Oculodigitoesophagoduodenal syndrome
A 0.700 CausalMutation CLINVAR
dbSNP: rs1553370260
rs1553370260
Entrez Id: 4613;10408
Gene Symbol: MYCN;MYCNOS
MYCN;MYCNOS
CUI: C0266174
Disease:
Duodenal atresia
ACTCG 0.700 CausalMutation CLINVAR
dbSNP: rs1553370260
rs1553370260
Entrez Id: 4613;10408
Gene Symbol: MYCN;MYCNOS
MYCN;MYCNOS
CUI: C4551774
Disease:
FEINGOLD SYNDROME 1
ACTCG 0.700 CausalMutation CLINVAR
dbSNP: rs1553370260
rs1553370260
Entrez Id: 4613;10408
Gene Symbol: MYCN;MYCNOS
MYCN;MYCNOS
CUI: C4551563
Disease:
Microcephaly (physical finding)
ACTCG 0.700 CausalMutation CLINVAR
dbSNP: rs1553370260
rs1553370260
Entrez Id: 4613;10408
Gene Symbol: MYCN;MYCNOS
MYCN;MYCNOS
CUI: C1859455
Disease:
Small anterior fontanelle
ACTCG 0.700 CausalMutation CLINVAR
dbSNP: rs1553370918
rs1553370918
Entrez Id: 4613
Gene Symbol: MYCN
MYCN
CUI: C0025990
Disease:
Micrognathism
C 0.700 CausalMutation CLINVAR
dbSNP: rs1553370918
rs1553370918
Entrez Id: 4613
Gene Symbol: MYCN
MYCN
CUI: C0039075
Disease:
Syndactyly
C 0.700 CausalMutation CLINVAR
dbSNP: rs1553370918
rs1553370918
Entrez Id: 4613
Gene Symbol: MYCN
MYCN
CUI: C4551774
Disease:
FEINGOLD SYNDROME 1
C 0.700 CausalMutation CLINVAR
dbSNP: rs1553370918
rs1553370918
Entrez Id: 4613
Gene Symbol: MYCN
MYCN
CUI: C0349588
Disease:
Short stature
C 0.700 CausalMutation CLINVAR
dbSNP: rs1553370918
rs1553370918
Entrez Id: 4613
Gene Symbol: MYCN
MYCN
CUI: C0014866
Disease:
Esophageal Stenosis
C 0.700 CausalMutation CLINVAR
dbSNP: rs1553370918
rs1553370918
Entrez Id: 4613
Gene Symbol: MYCN
MYCN
CUI: C4551563
Disease:
Microcephaly (physical finding)
C 0.700 CausalMutation CLINVAR
dbSNP: rs1553370963
rs1553370963
Entrez Id: 4613
Gene Symbol: MYCN
MYCN
CUI: C4551774
Disease:
FEINGOLD SYNDROME 1
GC 0.700 CausalMutation CLINVAR
dbSNP: rs1558534266
rs1558534266
Entrez Id: 4613;10408
Gene Symbol: MYCN;MYCNOS
MYCN;MYCNOS
CUI: C4551774
Disease:
FEINGOLD SYNDROME 1
GC 0.700 CausalMutation CLINVAR
dbSNP: rs367962377
rs367962377
Entrez Id: 4613
Gene Symbol: MYCN
MYCN
CUI: C4551774
Disease:
FEINGOLD SYNDROME 1
A 0.700 CausalMutation CLINVAR
dbSNP: rs367962377
rs367962377
Entrez Id: 4613
Gene Symbol: MYCN
MYCN
CUI: C4551563
Disease:
Microcephaly (physical finding)
A 0.700 CausalMutation CLINVAR
dbSNP: rs57961569
rs57961569
Entrez Id: 4613;10408
Gene Symbol: MYCN;MYCNOS
MYCN;MYCNOS
CUI: C1333015
Disease:
Childhood Kidney Wilms Tumor
0.010 GeneticVariation BEFREE Interestingly, in the stratification analysis, the rs57961569 was found to be associated with decreased Wilms tumor susceptibility in the children older than 18 months (AOR = 0.65, 95% CI = 0.42-1.00, P = .050). 31343784 2019
dbSNP: rs57961569
rs57961569
Entrez Id: 4613;10408
Gene Symbol: MYCN;MYCNOS
MYCN;MYCNOS
CUI: C0027708
Disease:
Nephroblastoma
0.010 GeneticVariation BEFREE Interestingly, in the stratification analysis, the rs57961569 was found to be associated with decreased Wilms tumor susceptibility in the children older than 18 months (AOR = 0.65, 95% CI = 0.42-1.00, P = .050). 31343784 2019
dbSNP: rs57961569
rs57961569
Entrez Id: 4613;10408
Gene Symbol: MYCN;MYCNOS
MYCN;MYCNOS
CUI: C0027819
Disease:
Neuroblastoma
0.010 GeneticVariation BEFREE Stratified analysis revealed that rs579</span>61569 GG carriers were more likely to develop neuroblastoma in the following subgroups: children older than 18 months, tumor derived from the adrenal gland, and clinical stages III + IV. 29997440 2018
dbSNP: rs57961569
rs57961569
Entrez Id: 4613;10408
Gene Symbol: MYCN;MYCNOS
MYCN;MYCNOS
CUI: C0700095
Disease:
Central neuroblastoma
0.010 GeneticVariation BEFREE Stratified analysis revealed that rs579</span>61569 GG carriers were more likely to develop neuroblastoma in the following subgroups: children older than 18 months, tumor derived from the adrenal gland, and clinical stages III + IV. 29997440 2018
dbSNP: rs57961569
rs57961569
Entrez Id: 4613;10408
Gene Symbol: MYCN;MYCNOS
MYCN;MYCNOS
CUI: C4086165
Disease:
Childhood Neuroblastoma
0.010 GeneticVariation BEFREE Stratified analysis revealed that rs579</span>61569 GG carriers were more likely to develop neuroblastoma in the following subgroups: children older than 18 months, tumor derived from the adrenal gland, and clinical stages III + IV. 29997440 2018
dbSNP: rs60226897
rs60226897
Entrez Id: 4613
Gene Symbol: MYCN
MYCN
CUI: C0700095
Disease:
Central neuroblastoma
0.010 GeneticVariation BEFREE The results showed that only rs57961569 G>A was associated with neuroblastoma risk (GA vs GG: adjusted odds ratio =0.76, 95% confidence interval =0.60-0.98, <i>P</i>=0.033), while the other 3 SNPs were not (rs9653226 T>C, rs13034994 A>G, and rs60226897 G>A). 29997440 2018
dbSNP: rs60226897
rs60226897
Entrez Id: 4613
Gene Symbol: MYCN
MYCN
CUI: C0027819
Disease:
Neuroblastoma
0.010 GeneticVariation BEFREE The results showed that only rs57961569 G>A was associated with neuroblastoma risk (GA vs GG: adjusted odds ratio =0.76, 95% confidence interval =0.60-0.98, <i>P</i>=0.033), while the other 3 SNPs were not (rs9653226 T>C, rs13034994 A>G, and rs60226897 G>A). 29997440 2018
dbSNP: rs60226897
rs60226897
Entrez Id: 4613
Gene Symbol: MYCN
MYCN
CUI: C4086165
Disease:
Childhood Neuroblastoma
0.010 GeneticVariation BEFREE The results showed that only rs57961569 G>A was associated with neuroblastoma risk (GA vs GG: adjusted odds ratio =0.76, 95% confidence interval =0.60-0.98, <i>P</i>=0.033), while the other 3 SNPs were not (rs9653226 T>C, rs13034994 A>G, and rs60226897 G>A). 29997440 2018
dbSNP: rs9653226
rs9653226
Entrez Id: 4613;10408
Gene Symbol: MYCN;MYCNOS
MYCN;MYCNOS
CUI: C0700095
Disease:
Central neuroblastoma
0.010 GeneticVariation BEFREE The results showed that only rs57961569 G>A was associated with neuroblastoma risk (GA vs GG: adjusted odds ratio =0.76, 95% confidence interval =0.60-0.98, <i>P</i>=0.033), while the other 3 SNPs were not (rs9653226 T>C, rs13034994 A>G, and rs60226897 G>A). 29997440 2018