Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs6939340
rs6939340
Entrez Id: 401237;729177
Gene Symbol: CASC15;NBAT1
CASC15;NBAT1
CUI: C0027819
Disease:
Neuroblastoma
0.840 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: rs6939340
rs6939340
Entrez Id: 401237;729177
Gene Symbol: CASC15;NBAT1
CASC15;NBAT1
CUI: C0027819
Disease:
Neuroblastoma
0.840 GeneticVariation BEFREE In the Henan population, only the rs6939340 G>A variant homozygote AA was associated with decreased neuroblastoma risk [AA vs. GG: adjusted odds ratio (OR) = 0.47, 95% confidence interval (CI) = 0.23-0.98; <i>P</i>=0.045]. 29207648 2017
dbSNP: rs6939340
rs6939340
Entrez Id: 401237;729177
Gene Symbol: CASC15;NBAT1
CASC15;NBAT1
CUI: C0027819
Disease:
Neuroblastoma
0.840 GeneticVariation BEFREE We found that the rs6939340 A allele carriers were associated with significantly decreased neuroblastoma susceptibility (AG vs. GG: adjusted OR = 0.54, 95 % CI = 0.38-0.77; AA vs. GG: adjusted OR = 0.49, 95 % CI = 0.25-0.93; and AA/AG vs. GG: adjusted OR = 0.53, 95 % CI = 0.38-0.74) after adjustment for age and gender. 26307394 2016
dbSNP: rs6939340
rs6939340
Entrez Id: 401237;729177
Gene Symbol: CASC15;NBAT1
CASC15;NBAT1
CUI: C0027819
Disease:
Neuroblastoma
0.840 GeneticVariation BEFREE Homozygosity for the at-risk G allele of the most significantly associated SNP, rs6939340, resulted in an increased likelihood of the development of neuroblastoma (odds ratio, 1.97; 95% confidence interval, 1.58 to 2.45). 18463370 2008
dbSNP: rs6939340
rs6939340
Entrez Id: 401237;729177
Gene Symbol: CASC15;NBAT1
CASC15;NBAT1
CUI: C0027819
Disease:
Neuroblastoma
G 0.840 GeneticVariation GWASDB Homozygosity for the at-risk G allele of the most significantly associated SNP, rs6939340, resulted in an increased likelihood of the development of neuroblastoma (odds ratio, 1.97; 95% confidence interval, 1.58 to 2.45). 18463370 2008
dbSNP: rs6939340
rs6939340
Entrez Id: 401237;729177
Gene Symbol: CASC15;NBAT1
CASC15;NBAT1
CUI: C0027819
Disease:
Neuroblastoma
G 0.840 GeneticVariation GWASCAT Homozygosity for the at-risk G allele of the most significantly associated SNP, rs6939340, resulted in an increased likelihood of the development of neuroblastoma (odds ratio, 1.97; 95% confidence interval, 1.58 to 2.45). 18463370 2008
dbSNP: rs4712656
rs4712656
Entrez Id: 401237;729177
Gene Symbol: CASC15;NBAT1
CASC15;NBAT1
CUI: C0014772
Disease:
Red Blood Cell Count measurement
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs4712656
rs4712656
Entrez Id: 401237;729177
Gene Symbol: CASC15;NBAT1
CASC15;NBAT1
CUI: C0428883
Disease:
Diastolic blood pressure
G 0.700 GeneticVariation GWASCAT Genome-wide association analyses using electronic health records identify new loci influencing blood pressure variation. 27841878 2017
dbSNP: rs4712656
rs4712656
Entrez Id: 401237;729177
Gene Symbol: CASC15;NBAT1
CASC15;NBAT1
CUI: C0871470
Disease:
Systolic Pressure
G 0.700 GeneticVariation GWASCAT Genome-wide association analyses using electronic health records identify new loci influencing blood pressure variation. 27841878 2017
dbSNP: rs4712656
rs4712656
Entrez Id: 401237;729177
Gene Symbol: CASC15;NBAT1
CASC15;NBAT1
CUI: C0027819
Disease:
Neuroblastoma
C 0.700 GeneticVariation GWASCAT Common variants upstream of MLF1 at 3q25 and within CPZ at 4p16 associated with neuroblastoma. 28545128 2017
dbSNP: rs6939340
rs6939340
Entrez Id: 401237;729177
Gene Symbol: CASC15;NBAT1
CASC15;NBAT1
CUI: C2931822
Disease:
Nasopharyngeal carcinoma
0.700 GeneticVariation GWASDB A genome-wide association study of nasopharyngeal carcinoma identifies three new susceptibility loci. 20512145 2010
dbSNP: rs6939340
rs6939340
Entrez Id: 401237;729177
Gene Symbol: CASC15;NBAT1
CASC15;NBAT1
CUI: C4086165
Disease:
Childhood Neuroblastoma
0.040 GeneticVariation BEFREE In the Henan population, only the rs6939340 G>A variant homozygote AA was associated with decreased neuroblastoma risk [AA vs. GG: adjusted odds ratio (OR) = 0.47, 95% confidence interval (CI) = 0.23-0.98; <i>P</i>=0.045]. 29207648 2017
dbSNP: rs6939340
rs6939340
Entrez Id: 401237;729177
Gene Symbol: CASC15;NBAT1
CASC15;NBAT1
CUI: C0700095
Disease:
Central neuroblastoma
0.040 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: rs6939340
rs6939340
Entrez Id: 401237;729177
Gene Symbol: CASC15;NBAT1
CASC15;NBAT1
CUI: C0700095
Disease:
Central neuroblastoma
0.040 GeneticVariation BEFREE In the Henan population, only the rs6939340 G>A variant homozygote AA was associated with decreased neuroblastoma risk [AA vs. GG: adjusted odds ratio (OR) = 0.47, 95% confidence interval (CI) = 0.23-0.98; <i>P</i>=0.045]. 29207648 2017
dbSNP: rs6939340
rs6939340
Entrez Id: 401237;729177
Gene Symbol: CASC15;NBAT1
CASC15;NBAT1
CUI: C4086165
Disease:
Childhood Neuroblastoma
0.040 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: rs6939340
rs6939340
Entrez Id: 401237;729177
Gene Symbol: CASC15;NBAT1
CASC15;NBAT1
CUI: C0700095
Disease:
Central neuroblastoma
0.040 GeneticVariation BEFREE We found that the rs6939340 A allele carriers were associated with significantly decreased neuroblastoma susceptibility (AG vs. GG: adjusted OR = 0.54, 95 % CI = 0.38-0.77; AA vs. GG: adjusted OR = 0.49, 95 % CI = 0.25-0.93; and AA/AG vs. GG: adjusted OR = 0.53, 95 % CI = 0.38-0.74) after adjustment for age and gender. 26307394 2016
dbSNP: rs6939340
rs6939340
Entrez Id: 401237;729177
Gene Symbol: CASC15;NBAT1
CASC15;NBAT1
CUI: C4086165
Disease:
Childhood Neuroblastoma
0.040 GeneticVariation BEFREE We found that the rs6939340 A allele carriers were associated with significantly decreased neuroblastoma susceptibility (AG vs. GG: adjusted OR = 0.54, 95 % CI = 0.38-0.77; AA vs. GG: adjusted OR = 0.49, 95 % CI = 0.25-0.93; and AA/AG vs. GG: adjusted OR = 0.53, 95 % CI = 0.38-0.74) after adjustment for age and gender. 26307394 2016
dbSNP: rs6939340
rs6939340
Entrez Id: 401237;729177
Gene Symbol: CASC15;NBAT1
CASC15;NBAT1
CUI: C0700095
Disease:
Central neuroblastoma
0.040 GeneticVariation BEFREE Homozygosity for the at-risk G allele of the most significantly associated SNP, rs6939340, resulted in an increased likelihood of the development of neuroblastoma (odds ratio, 1.97; 95% confidence interval, 1.58 to 2.45). 18463370 2008
dbSNP: rs6939340
rs6939340
Entrez Id: 401237;729177
Gene Symbol: CASC15;NBAT1
CASC15;NBAT1
CUI: C4086165
Disease:
Childhood Neuroblastoma
0.040 GeneticVariation BEFREE Homozygosity for the at-risk G allele of the most significantly associated SNP, rs6939340, resulted in an increased likelihood of the development of neuroblastoma (odds ratio, 1.97; 95% confidence interval, 1.58 to 2.45). 18463370 2008