Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1057519895
rs1057519895
Entrez Id: 55294
Gene Symbol: FBXW7
FBXW7
CUI: C0025149
Disease:
Medulloblastoma 		A 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
dbSNP: rs1057519895
rs1057519895
Entrez Id: 55294
Gene Symbol: FBXW7
FBXW7
CUI: C0023434
Disease:
Chronic Lymphocytic Leukemia 		T 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
dbSNP: rs1057519895
rs1057519895
Entrez Id: 55294
Gene Symbol: FBXW7
FBXW7
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: rs1057519895
rs1057519895
Entrez Id: 55294
Gene Symbol: FBXW7
FBXW7
CUI: C0023434
Disease:
Chronic Lymphocytic Leukemia 		G 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
dbSNP: rs1057519895
rs1057519895
Entrez Id: 55294
Gene Symbol: FBXW7
FBXW7
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: rs1057519895
rs1057519895
Entrez Id: 55294
Gene Symbol: FBXW7
FBXW7
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: rs1057519895
rs1057519895
Entrez Id: 55294
Gene Symbol: FBXW7
FBXW7
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: rs1057519895
rs1057519895
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: rs1057519895
rs1057519895
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: rs1057519895
rs1057519895
Entrez Id: 55294
Gene Symbol: FBXW7
FBXW7
CUI: C0009404
Disease:
Colorectal Neoplasms 		A 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
dbSNP: rs1057519895
rs1057519895
Entrez Id: 55294
Gene Symbol: FBXW7
FBXW7
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: rs1057519895
rs1057519895
Entrez Id: 55294
Gene Symbol: FBXW7
FBXW7
CUI: C0010606
Disease:
Adenoid Cystic Carcinoma 		G 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
dbSNP: rs1057519895
rs1057519895
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: rs1057519895
rs1057519895
Entrez Id: 55294
Gene Symbol: FBXW7
FBXW7
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: rs1057519895
rs1057519895
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: rs1057519895
rs1057519895
Entrez Id: 55294
Gene Symbol: FBXW7
FBXW7
CUI: C0278701
Disease:
Gastric Adenocarcinoma 		G 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
dbSNP: rs1057519895
rs1057519895
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: rs1057519895
rs1057519895
Entrez Id: 55294
Gene Symbol: FBXW7
FBXW7
CUI: C0152018
Disease:
Esophageal carcinoma 		G 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
dbSNP: rs1057519895
rs1057519895
Entrez Id: 55294
Gene Symbol: FBXW7
FBXW7
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: rs1057519895
rs1057519895
Entrez Id: 55294
Gene Symbol: FBXW7
FBXW7
CUI: C1458155
Disease:
Mammary Neoplasms 		G 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
dbSNP: rs1057519895
rs1057519895
Entrez Id: 55294
Gene Symbol: FBXW7
FBXW7
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: rs1057519895
rs1057519895
Entrez Id: 55294
Gene Symbol: FBXW7
FBXW7
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: rs1057519896
rs1057519896
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: rs1057519896
rs1057519896
Entrez Id: 55294
Gene Symbol: FBXW7
FBXW7
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: rs1057519896
rs1057519896
Entrez Id: 55294
Gene Symbol: FBXW7
FBXW7
CUI: C0151779
Disease:
Cutaneous Melanoma 		A 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016