rs747418061, APC

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.
Activated Protein C Resistance
CUI: C0600433
Disease: Activated Protein C Resistance
30 0.807 0.200 5 112828920 missense variant G/A snv 3.2E-05 7.0E-06 0.070 1.000 7 1995 2010
Factor V Leiden mutation
CUI: C0584960
Disease: Factor V Leiden mutation
46 0.807 0.200 5 112828920 missense variant G/A snv 3.2E-05 7.0E-06 0.040 1.000 4 1995 2017
Thrombophilia
CUI: C0398623
Disease: Thrombophilia
43 0.807 0.200 5 112828920 missense variant G/A snv 3.2E-05 7.0E-06 0.030 1.000 3 1997 2005
Venous Thromboembolism
CUI: C1861172
Disease: Venous Thromboembolism
408 0.807 0.200 5 112828920 missense variant G/A snv 3.2E-05 7.0E-06 0.020 1.000 2 1995 2003
Deep Vein Thrombosis
CUI: C0149871
Disease: Deep Vein Thrombosis
93 0.807 0.200 5 112828920 missense variant G/A snv 3.2E-05 7.0E-06 0.010 1.000 1 1998 1998
Fetal Growth Retardation
CUI: C0015934
Disease: Fetal Growth Retardation
21 0.807 0.200 5 112828920 missense variant G/A snv 3.2E-05 7.0E-06 0.010 1.000 1 1998 1998
Ischemic stroke
CUI: C0948008
Disease: Ischemic stroke
704 0.807 0.200 5 112828920 missense variant G/A snv 3.2E-05 7.0E-06 0.010 1.000 1 1999 1999
Miscarriage
CUI: C4552766
Disease: Miscarriage
56 0.807 0.200 5 112828920 missense variant G/A snv 3.2E-05 7.0E-06 0.010 1.000 1 2005 2005
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.807 0.200 5 112828920 missense variant G/A snv 3.2E-05 7.0E-06 0.010 1.000 1 2015 2015
Venoocclusive disease
CUI: C0948441
Disease: Venoocclusive disease
4 0.807 0.200 5 112828920 missense variant G/A snv 3.2E-05 7.0E-06 0.010 1.000 1 1997 1997