Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1057519851
rs1057519851
Entrez Id: 4609
Gene Symbol: MYC
MYC
CUI: C0027651
Disease:
Neoplasms 		G 0.700 GeneticVariation CLINVAR Prospective enterprise-level molecular genotyping of a cohort of cancer patients. 25157968 2014
dbSNP: rs2070583
rs2070583
Entrez Id: 4609
Gene Symbol: MYC
MYC
CUI: C0010068
Disease:
Coronary heart disease 		0.010 GeneticVariation BEFREE We also identified a SNP achieving array wide significance (MYC: rs2070583, allele frequency 0.02, P = 8.1 × 10(-8)), but the association did not replicate in an additional 8,059 African Americans (577 events) from the WHI, HealthABC and GeneSTAR studies, and in a meta-analysis of 5 cohort studies of European ancestry (24,024 individuals including 1,570 cases of MI and 2,406 cases of CHD) from the CHARGE Consortium. 25542012 2014
dbSNP: rs1057519849
rs1057519849
Entrez Id: 4609;100270680
Gene Symbol: MYC;CASC11
MYC;CASC11
CUI: C0027651
Disease:
Neoplasms 		T 0.700 GeneticVariation CLINVAR Prospective enterprise-level molecular genotyping of a cohort of cancer patients. 25157968 2014
dbSNP: rs1057519850
rs1057519850
Entrez Id: 4609;100270680
Gene Symbol: MYC;CASC11
MYC;CASC11
CUI: C0027651
Disease:
Neoplasms 		T 0.700 GeneticVariation CLINVAR Prospective enterprise-level molecular genotyping of a cohort of cancer patients. 25157968 2014
dbSNP: rs1057519918
rs1057519918
Entrez Id: 4609;100270680
Gene Symbol: MYC;CASC11
MYC;CASC11
CUI: C0151779
Disease:
Cutaneous Melanoma 		T 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
dbSNP: rs1057519918
rs1057519918
Entrez Id: 4609;100270680
Gene Symbol: MYC;CASC11
MYC;CASC11
CUI: C4721532
Disease:
Lymphoma, Non-Hodgkin, Familial 		T 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
dbSNP: rs1057519918
rs1057519918
Entrez Id: 4609;100270680
Gene Symbol: MYC;CASC11
MYC;CASC11
CUI: C0152013
Disease:
Adenocarcinoma of lung (disorder) 		T 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
dbSNP: rs1057519918
rs1057519918
Entrez Id: 4609;100270680
Gene Symbol: MYC;CASC11
MYC;CASC11
CUI: C2749484
Disease:
NEUROBLASTOMA, SUSCEPTIBILITY TO 		T 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
dbSNP: rs1057519918
rs1057519918
Entrez Id: 4609;100270680
Gene Symbol: MYC;CASC11
MYC;CASC11
CUI: C0152018
Disease:
Esophageal carcinoma 		T 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
dbSNP: rs121918683
rs121918683
Entrez Id: 4609;100270680
Gene Symbol: MYC;CASC11
MYC;CASC11
CUI: C0027651
Disease:
Neoplasms 		C 0.700 GeneticVariation CLINVAR Prospective enterprise-level molecular genotyping of a cohort of cancer patients. 25157968 2014
dbSNP: rs121918683
rs121918683
Entrez Id: 4609;100270680
Gene Symbol: MYC;CASC11
MYC;CASC11
CUI: C0006413
Disease:
Burkitt Lymphoma 		0.700 GeneticVariation UNIPROT
dbSNP: rs121918685
rs121918685
Entrez Id: 4609;100270680
Gene Symbol: MYC;CASC11
MYC;CASC11
CUI: C0006413
Disease:
Burkitt Lymphoma 		0.700 GeneticVariation UNIPROT
dbSNP: rs28933407
rs28933407
Entrez Id: 4609;100270680
Gene Symbol: MYC;CASC11
MYC;CASC11
CUI: C0006413
Disease:
Burkitt Lymphoma 		0.700 GeneticVariation UNIPROT
dbSNP: rs750664148
rs750664148
Entrez Id: 4609;100270680
Gene Symbol: MYC;CASC11
MYC;CASC11
CUI: C0151779
Disease:
Cutaneous Melanoma 		C 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
dbSNP: rs750664148
rs750664148
Entrez Id: 4609;100270680
Gene Symbol: MYC;CASC11
MYC;CASC11
CUI: C0152013
Disease:
Adenocarcinoma of lung (disorder) 		C 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
dbSNP: rs750664148
rs750664148
Entrez Id: 4609;100270680
Gene Symbol: MYC;CASC11
MYC;CASC11
CUI: C2749484
Disease:
NEUROBLASTOMA, SUSCEPTIBILITY TO 		C 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
dbSNP: rs750664148
rs750664148
Entrez Id: 4609;100270680
Gene Symbol: MYC;CASC11
MYC;CASC11
CUI: C4721532
Disease:
Lymphoma, Non-Hodgkin, Familial 		C 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
dbSNP: rs750664148
rs750664148
Entrez Id: 4609;100270680
Gene Symbol: MYC;CASC11
MYC;CASC11
CUI: C0152018
Disease:
Esophageal carcinoma 		C 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
dbSNP: rs756091827
rs756091827
Entrez Id: 4609;100270680
Gene Symbol: MYC;CASC11
MYC;CASC11
CUI: C2749484
Disease:
NEUROBLASTOMA, SUSCEPTIBILITY TO 		T 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
dbSNP: rs756091827
rs756091827
Entrez Id: 4609;100270680
Gene Symbol: MYC;CASC11
MYC;CASC11
CUI: C0152013
Disease:
Adenocarcinoma of lung (disorder) 		T 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
dbSNP: rs756091827
rs756091827
Entrez Id: 4609;100270680
Gene Symbol: MYC;CASC11
MYC;CASC11
CUI: C0027651
Disease:
Neoplasms 		T 0.700 GeneticVariation CLINVAR Prospective enterprise-level molecular genotyping of a cohort of cancer patients. 25157968 2014
dbSNP: rs756091827
rs756091827
Entrez Id: 4609;100270680
Gene Symbol: MYC;CASC11
MYC;CASC11
CUI: C0152018
Disease:
Esophageal carcinoma 		T 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
dbSNP: rs756091827
rs756091827
Entrez Id: 4609;100270680
Gene Symbol: MYC;CASC11
MYC;CASC11
CUI: C0151779
Disease:
Cutaneous Melanoma 		T 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
dbSNP: rs756091827
rs756091827
Entrez Id: 4609;100270680
Gene Symbol: MYC;CASC11
MYC;CASC11
CUI: C4721532
Disease:
Lymphoma, Non-Hodgkin, Familial 		T 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
dbSNP: rs775522201
rs775522201
Entrez Id: 4609;100270680
Gene Symbol: MYC;CASC11
MYC;CASC11
CUI: C0027651
Disease:
Neoplasms 		T 0.700 GeneticVariation CLINVAR Prospective enterprise-level molecular genotyping of a cohort of cancer patients. 25157968 2014