Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1057519896
rs1057519896
Entrez Id: 55294
Gene Symbol: FBXW7
FBXW7
CUI: C0023434
Disease:
Chronic Lymphocytic Leukemia 		A 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
dbSNP: rs1057519896
rs1057519896
Entrez Id: 55294
Gene Symbol: FBXW7
FBXW7
CUI: C0279663
Disease:
Serous cystadenocarcinoma ovary 		A 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
dbSNP: rs1057519896
rs1057519896
Entrez Id: 55294
Gene Symbol: FBXW7
FBXW7
CUI: C0278701
Disease:
Gastric Adenocarcinoma 		A 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
dbSNP: rs1057519896
rs1057519896
Entrez Id: 55294
Gene Symbol: FBXW7
FBXW7
CUI: C0280630
Disease:
Uterine Carcinosarcoma 		A 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
dbSNP: rs1057519896
rs1057519896
Entrez Id: 55294
Gene Symbol: FBXW7
FBXW7
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: rs1057519896
rs1057519896
Entrez Id: 55294
Gene Symbol: FBXW7
FBXW7
CUI: C0152018
Disease:
Esophageal carcinoma 		A 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
dbSNP: rs1057519896
rs1057519896
Entrez Id: 55294
Gene Symbol: FBXW7
FBXW7
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: rs1057519896
rs1057519896
Entrez Id: 55294
Gene Symbol: FBXW7
FBXW7
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: rs149680468
rs149680468
Entrez Id: 55294
Gene Symbol: FBXW7
FBXW7
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: rs149680468
rs149680468
Entrez Id: 55294
Gene Symbol: FBXW7
FBXW7
CUI: C0152018
Disease:
Esophageal carcinoma 		A 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
dbSNP: rs149680468
rs149680468
Entrez Id: 55294
Gene Symbol: FBXW7
FBXW7
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: rs149680468
rs149680468
Entrez Id: 55294
Gene Symbol: FBXW7
FBXW7
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: rs149680468
rs149680468
Entrez Id: 55294
Gene Symbol: FBXW7
FBXW7
CUI: C0280630
Disease:
Uterine Carcinosarcoma 		T 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
dbSNP: rs149680468
rs149680468
Entrez Id: 55294
Gene Symbol: FBXW7
FBXW7
CUI: C0023434
Disease:
Chronic Lymphocytic Leukemia 		A 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
dbSNP: rs149680468
rs149680468
Entrez Id: 55294
Gene Symbol: FBXW7
FBXW7
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: rs149680468
rs149680468
Entrez Id: 55294
Gene Symbol: FBXW7
FBXW7
CUI: C0279663
Disease:
Serous cystadenocarcinoma ovary 		C 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
dbSNP: rs149680468
rs149680468
Entrez Id: 55294
Gene Symbol: FBXW7
FBXW7
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: rs149680468
rs149680468
Entrez Id: 55294
Gene Symbol: FBXW7
FBXW7
CUI: C0280630
Disease:
Uterine Carcinosarcoma 		C 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
dbSNP: rs149680468
rs149680468
Entrez Id: 55294
Gene Symbol: FBXW7
FBXW7
CUI: C0009404
Disease:
Colorectal Neoplasms 		T 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
dbSNP: rs149680468
rs149680468
Entrez Id: 55294
Gene Symbol: FBXW7
FBXW7
CUI: C0278701
Disease:
Gastric Adenocarcinoma 		A 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
dbSNP: rs149680468
rs149680468
Entrez Id: 55294
Gene Symbol: FBXW7
FBXW7
CUI: C0279663
Disease:
Serous cystadenocarcinoma ovary 		A 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
dbSNP: rs149680468
rs149680468
Entrez Id: 55294
Gene Symbol: FBXW7
FBXW7
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: rs149680468
rs149680468
Entrez Id: 55294
Gene Symbol: FBXW7
FBXW7
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: rs149680468
rs149680468
Entrez Id: 55294
Gene Symbol: FBXW7
FBXW7
CUI: C0279663
Disease:
Serous cystadenocarcinoma ovary 		T 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
dbSNP: rs149680468
rs149680468
Entrez Id: 55294
Gene Symbol: FBXW7
FBXW7
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