Source: GWASCAT

Gene Gene Full Name DSI g DPI g pLI Disease Type Score gda EL gda EI gda N. PMIDs N. SNPs gda First Ref. Last Ref.
Entrez Id: 2153
Gene Symbol: F5
F5
coagulation factor V 0.441 0.846 5.9E-15
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism
phenotype 0.500 None 0.964 8 4 1995 2020
Entrez Id: 2153
Gene Symbol: F5
F5
coagulation factor V 0.441 0.846 5.9E-15
CUI: C0038454
Disease: Cerebrovascular accident
Cerebrovascular accident
group 0.500 None 0.971 1 1 1995 2016
Entrez Id: 2153
Gene Symbol: F5
F5
coagulation factor V 0.441 0.846 5.9E-15
CUI: C0149871
Disease: Deep Vein Thrombosis
Deep Vein Thrombosis
disease 0.500 None 1.000 1 1 1996 2018
Entrez Id: 2153
Gene Symbol: F5
F5
coagulation factor V 0.441 0.846 5.9E-15
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases
group 0.200 None 0.909 1 1 1998 2015
Entrez Id: 2153
Gene Symbol: F5
F5
coagulation factor V 0.441 0.846 5.9E-15
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke
disease 0.200 None 0.962 1 1 1998 2019
Entrez Id: 2153
Gene Symbol: F5
F5
coagulation factor V 0.441 0.846 5.9E-15
CUI: C0034065
Disease: Pulmonary Embolism
Pulmonary Embolism
disease 0.120 None 1.000 1 1 2002 2016
Entrez Id: 2153
Gene Symbol: F5
F5
coagulation factor V 0.441 0.846 5.9E-15
CUI: C1704436
Disease: Peripheral Arterial Diseases
Peripheral Arterial Diseases
group 0.120 None 1.000 1 1 2005 2019
Entrez Id: 2153
Gene Symbol: F5
F5
coagulation factor V 0.441 0.846 5.9E-15
Activated Partial Thromboplastin Time measurement
phenotype 0.100 None 1.000 2 2 2012 2018
Entrez Id: 2153
Gene Symbol: F5
F5
coagulation factor V 0.441 0.846 5.9E-15
CUI: C2825910
Disease: Stem Cell Factor Measurement
Stem Cell Factor Measurement
phenotype 0.100 None 1.000 1 1 2017 2017
Entrez Id: 2153
Gene Symbol: F5
F5
coagulation factor V 0.441 0.846 5.9E-15
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement
phenotype 0.100 None 1.000 1 9 2018 2018
Entrez Id: 2153
Gene Symbol: F5
F5
coagulation factor V 0.441 0.846 5.9E-15
CUI: C4315130
Disease: Hippocampal atrophy
Hippocampal atrophy
phenotype 0.100 None 1.000 1 1 2012 2012