NFE2L2, nuclear factor, erythroid 2 like 2, 4780

N. diseases: 823; N. variants: 34
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs10497511
rs10497511
Entrez Id: 4780
Gene Symbol: NFE2L2
NFE2L2
CUI: C0011860
Disease:
Diabetes Mellitus, Non-Insulin-Dependent 		0.010 GeneticVariation BEFREE The data suggest that although NFE2L2 rs2364723, rs10497511, rs1962142 and rs6726395 were not associated with T2DM risk, they were significantly associated with complications of T2DM. 27374075 2016
dbSNP: rs1057519920
rs1057519920
Entrez Id: 4780
Gene Symbol: NFE2L2
NFE2L2
CUI: C0279680
Disease:
Transitional cell carcinoma of bladder 		T 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
dbSNP: rs1057519920
rs1057519920
Entrez Id: 4780
Gene Symbol: NFE2L2
NFE2L2
CUI: C0153574
Disease:
Malignant Uterine Corpus Neoplasm 		A 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
dbSNP: rs1057519920
rs1057519920
Entrez Id: 4780
Gene Symbol: NFE2L2
NFE2L2
CUI: C0007873
Disease:
Uterine Cervical Neoplasm 		T 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
dbSNP: rs1057519920
rs1057519920
Entrez Id: 4780
Gene Symbol: NFE2L2
NFE2L2
CUI: C0007134
Disease:
Renal Cell Carcinoma 		A 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
dbSNP: rs1057519920
rs1057519920
Entrez Id: 4780
Gene Symbol: NFE2L2
NFE2L2
CUI: C1168401
Disease:
Squamous cell carcinoma of the head and neck 		T 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
dbSNP: rs1057519920
rs1057519920
Entrez Id: 4780
Gene Symbol: NFE2L2
NFE2L2
CUI: C0149782
Disease:
Squamous cell carcinoma of lung 		G 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
dbSNP: rs1057519920
rs1057519920
Entrez Id: 4780
Gene Symbol: NFE2L2
NFE2L2
CUI: C0007873
Disease:
Uterine Cervical Neoplasm 		G 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
dbSNP: rs1057519920
rs1057519920
Entrez Id: 4780
Gene Symbol: NFE2L2
NFE2L2
CUI: C0153574
Disease:
Malignant Uterine Corpus Neoplasm 		G 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
dbSNP: rs1057519920
rs1057519920
Entrez Id: 4780
Gene Symbol: NFE2L2
NFE2L2
CUI: C0152013
Disease:
Adenocarcinoma of lung (disorder) 		G 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
dbSNP: rs1057519920
rs1057519920
Entrez Id: 4780
Gene Symbol: NFE2L2
NFE2L2
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: rs1057519920
rs1057519920
Entrez Id: 4780
Gene Symbol: NFE2L2
NFE2L2
CUI: C0007873
Disease:
Uterine Cervical Neoplasm 		A 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
dbSNP: rs1057519920
rs1057519920
Entrez Id: 4780
Gene Symbol: NFE2L2
NFE2L2
CUI: C1168401
Disease:
Squamous cell carcinoma of the head and neck 		G 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
dbSNP: rs1057519920
rs1057519920
Entrez Id: 4780
Gene Symbol: NFE2L2
NFE2L2
CUI: C0152013
Disease:
Adenocarcinoma of lung (disorder) 		A 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
dbSNP: rs1057519920
rs1057519920
Entrez Id: 4780
Gene Symbol: NFE2L2
NFE2L2
CUI: C0279680
Disease:
Transitional cell carcinoma of bladder 		A 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
dbSNP: rs1057519920
rs1057519920
Entrez Id: 4780
Gene Symbol: NFE2L2
NFE2L2
CUI: C0279680
Disease:
Transitional cell carcinoma of bladder 		G 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
dbSNP: rs1057519920
rs1057519920
Entrez Id: 4780
Gene Symbol: NFE2L2
NFE2L2
CUI: C0007134
Disease:
Renal Cell Carcinoma 		G 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
dbSNP: rs1057519920
rs1057519920
Entrez Id: 4780
Gene Symbol: NFE2L2
NFE2L2
CUI: C0153574
Disease:
Malignant Uterine Corpus Neoplasm 		T 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
dbSNP: rs1057519920
rs1057519920
Entrez Id: 4780
Gene Symbol: NFE2L2
NFE2L2
CUI: C0007134
Disease:
Renal Cell Carcinoma 		T 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
dbSNP: rs1057519920
rs1057519920
Entrez Id: 4780
Gene Symbol: NFE2L2
NFE2L2
CUI: C1168401
Disease:
Squamous cell carcinoma of the head and neck 		A 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
dbSNP: rs1057519920
rs1057519920
Entrez Id: 4780
Gene Symbol: NFE2L2
NFE2L2
CUI: C0149782
Disease:
Squamous cell carcinoma of lung 		A 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
dbSNP: rs1057519920
rs1057519920
Entrez Id: 4780
Gene Symbol: NFE2L2
NFE2L2
CUI: C0149782
Disease:
Squamous cell carcinoma of lung 		T 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
dbSNP: rs1057519921
rs1057519921
Entrez Id: 4780
Gene Symbol: NFE2L2
NFE2L2
CUI: C0153574
Disease:
Malignant Uterine Corpus Neoplasm 		C 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
dbSNP: rs1057519921
rs1057519921
Entrez Id: 4780
Gene Symbol: NFE2L2
NFE2L2
CUI: C0007134
Disease:
Renal Cell Carcinoma 		C 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
dbSNP: rs1057519921
rs1057519921
Entrez Id: 4780
Gene Symbol: NFE2L2
NFE2L2
CUI: C0149782
Disease:
Squamous cell carcinoma of lung 		C 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016