Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs2066865
rs2066865
FGG
0.807 0.240 4 154604124 downstream gene variant G/A snv 0.26
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism 		0.860 0.900 6 2011 2019
dbSNP: rs2066865
rs2066865
FGG
0.807 0.240 4 154604124 downstream gene variant G/A snv 0.26
CUI: C0149871
Disease: Deep Vein Thrombosis
Deep Vein Thrombosis 		0.020 1.000 2 2007 2010
dbSNP: rs1049636
rs1049636
FGG
1.000 0.080 4 154604818 3 prime UTR variant G/A snv 0.67 0.70
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		0.010 1.000 1 2007 2007
dbSNP: rs121913087
rs121913087
FGG
0.925 0.080 4 154606933 missense variant G/A snv
CUI: C1260903
Disease: Dysfibrinogenemia
Dysfibrinogenemia 		0.010 1.000 1 2015 2015
dbSNP: rs121913091
rs121913091
FGG
1.000 0.080 4 154606827 missense variant A/G snv
CUI: C0272350
Disease: Dysfibrinogenemia, Congenital
Dysfibrinogenemia, Congenital 		0.010 1.000 1 2009 2009
dbSNP: rs2066865
rs2066865
FGG
0.807 0.240 4 154604124 downstream gene variant G/A snv 0.26
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.010 1.000 1 2010 2010
dbSNP: rs2066865
rs2066865
FGG
0.807 0.240 4 154604124 downstream gene variant G/A snv 0.26
CUI: C1961102
Disease: Precursor Cell Lymphoblastic Leukemia Lymphoma
Precursor Cell Lymphoblastic Leukemia Lymphoma 		0.010 1.000 1 2019 2019
dbSNP: rs2066865
rs2066865
FGG
0.807 0.240 4 154604124 downstream gene variant G/A snv 0.26
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		0.010 1.000 1 2019 2019
dbSNP: rs2066865
rs2066865
FGG
0.807 0.240 4 154604124 downstream gene variant G/A snv 0.26
CUI: C0584960
Disease: Factor V Leiden mutation
Factor V Leiden mutation 		0.010 1.000 1 2012 2012
dbSNP: rs2066865
rs2066865
FGG
0.807 0.240 4 154604124 downstream gene variant G/A snv 0.26
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm 		0.010 1.000 1 2019 2019
dbSNP: rs2066865
rs2066865
FGG
0.807 0.240 4 154604124 downstream gene variant G/A snv 0.26
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		0.010 1.000 1 2010 2010
dbSNP: rs2066865
rs2066865
FGG
0.807 0.240 4 154604124 downstream gene variant G/A snv 0.26
CUI: C0023449
Disease: Acute lymphocytic leukemia
Acute lymphocytic leukemia 		0.010 1.000 1 2019 2019
dbSNP: rs75848804
rs75848804
FGG
0.882 0.080 4 154604995 missense variant G/A;C;T snv
CUI: C0267971
Disease: Storage disease
Storage disease 		0.010 1.000 1 2006 2006
dbSNP: rs75848804
rs75848804
FGG
0.882 0.080 4 154604995 missense variant G/A;C;T snv
CUI: C4316812
Disease: Fibrinogen Deficiency
Fibrinogen Deficiency 		0.010 1.000 1 2015 2015
dbSNP: rs75848804
rs75848804
FGG
0.882 0.080 4 154604995 missense variant G/A;C;T snv
CUI: C0553681
Disease: Hypofibrinogenemia
Hypofibrinogenemia 		0.010 1.000 1 2015 2015