rs1312546120, F5

N. diseases: 7
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.
Factor V Leiden mutation
CUI: C0584960
Disease: Factor V Leiden mutation
46 0.807 0.160 1 169541191 missense variant T/C snv 4.0E-06 0.020 1.000 2 2004 2019
Activated Protein C Resistance
CUI: C0600433
Disease: Activated Protein C Resistance
30 0.807 0.160 1 169541191 missense variant T/C snv 4.0E-06 0.010 1.000 1 2004 2004
Factor II mutation
CUI: C1610621
Disease: Factor II mutation
2 0.807 0.160 1 169541191 missense variant T/C snv 4.0E-06 0.010 1.000 1 2012 2012
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.807 0.160 1 169541191 missense variant T/C snv 4.0E-06 0.010 1.000 1 2000 2000
Thrombophilia
CUI: C0398623
Disease: Thrombophilia
43 0.807 0.160 1 169541191 missense variant T/C snv 4.0E-06 0.010 1.000 1 2018 2018
Thrombophilia, hereditary
CUI: C2584620
Disease: Thrombophilia, hereditary
9 0.807 0.160 1 169541191 missense variant T/C snv 4.0E-06 0.010 1.000 1 2012 2012
Venous Thromboembolism
CUI: C1861172
Disease: Venous Thromboembolism
408 0.807 0.160 1 169541191 missense variant T/C snv 4.0E-06 0.010 1.000 1 2008 2008