Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2203644
rs2203644
Entrez Id: 55294
Gene Symbol: FBXW7
FBXW7
CUI: C0200638
Disease:
Eosinophil count procedure 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs7660590
rs7660590
Entrez Id: 55294
Gene Symbol: FBXW7
FBXW7
CUI: C0011860
Disease:
Diabetes Mellitus, Non-Insulin-Dependent 		C 0.700 GeneticVariation GWASCAT Identification of 28 new susceptibility loci for type 2 diabetes in the Japanese population. 30718926 2019
dbSNP: rs4315757
rs4315757
Entrez Id: 55294
Gene Symbol: FBXW7
FBXW7
CUI: C0410702
Disease:
Adolescent idiopathic scoliosis 		0.700 GeneticVariation GWASCAT The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease. 30019117 2018
dbSNP: rs4315757
rs4315757
Entrez Id: 55294
Gene Symbol: FBXW7
FBXW7
CUI: C1837461
Disease:
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		0.700 GeneticVariation GWASCAT The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease. 30019117 2018
dbSNP: rs7685296
rs7685296
Entrez Id: 55294
Gene Symbol: FBXW7
FBXW7
CUI: C0011860
Disease:
Diabetes Mellitus, Non-Insulin-Dependent 		T 0.700 GeneticVariation GWASCAT Genome-wide association analyses identify 143 risk variants and putative regulatory mechanisms for type 2 diabetes. 30054458 2018
dbSNP: rs1057519895
rs1057519895
Entrez Id: 55294
Gene Symbol: FBXW7
FBXW7
CUI: C0280630
Disease:
Uterine Carcinosarcoma 		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: C0278701
Disease:
Gastric Adenocarcinoma 		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 		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: C0278701
Disease:
Gastric Adenocarcinoma 		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: 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: rs1057519895
rs1057519895
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: rs1057519895
rs1057519895
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: rs1057519895
rs1057519895
Entrez Id: 55294
Gene Symbol: FBXW7
FBXW7
CUI: C0279663
Disease:
Serous cystadenocarcinoma ovary 		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: C0010606
Disease:
Adenoid Cystic Carcinoma 		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: C0152018
Disease:
Esophageal carcinoma 		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: C0010606
Disease:
Adenoid Cystic 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: C0025149
Disease:
Medulloblastoma 		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 		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: C1458155
Disease:
Mammary 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: C0280630
Disease:
Uterine Carcinosarcoma 		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: C0025149
Disease:
Medulloblastoma 		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: C1458155
Disease:
Mammary 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: C0280630
Disease:
Uterine Carcinosarcoma 		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: 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: rs1057519895
rs1057519895
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