rs2066865, FGG

N. diseases: 10
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Venous Thromboembolism
CUI: C1861172
Disease: Venous Thromboembolism
408 0.807 0.240 4 154604124 downstream gene variant G/A snv 0.26 0.860 0.900 10 2011 2019
Venous Thrombosis
CUI: C0042487
Disease: Venous Thrombosis
218 0.807 0.240 4 154604124 downstream gene variant G/A snv 0.26 0.700 1.000 1 2012 2012
Deep Vein Thrombosis
CUI: C0149871
Disease: Deep Vein Thrombosis
93 0.807 0.240 4 154604124 downstream gene variant G/A snv 0.26 0.020 1.000 2 2007 2010
Acute lymphocytic leukemia
CUI: C0023449
Disease: Acute lymphocytic leukemia
222 0.807 0.240 4 154604124 downstream gene variant G/A snv 0.26 0.010 1.000 1 2019 2019
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.807 0.240 4 154604124 downstream gene variant G/A snv 0.26 0.010 1.000 1 2010 2010
Factor V Leiden mutation
CUI: C0584960
Disease: Factor V Leiden mutation
46 0.807 0.240 4 154604124 downstream gene variant G/A snv 0.26 0.010 1.000 1 2012 2012
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.807 0.240 4 154604124 downstream gene variant G/A snv 0.26 0.010 1.000 1 2019 2019
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.807 0.240 4 154604124 downstream gene variant G/A snv 0.26 0.010 1.000 1 2010 2010
Precursor Cell Lymphoblastic Leukemia Lymphoma
CUI: C1961102
Disease: Precursor Cell Lymphoblastic Leukemia Lymphoma
168 0.807 0.240 4 154604124 downstream gene variant G/A snv 0.26 0.010 1.000 1 2019 2019
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.807 0.240 4 154604124 downstream gene variant G/A snv 0.26 0.010 1.000 1 2019 2019