rs121918474, PROS1

N. diseases: 11
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.
THROMBOPHILIA DUE TO PROTEIN S DEFICIENCY, AUTOSOMAL DOMINANT
38 0.763 0.320 3 93905799 missense variant T/C snv 2.8E-05 1.4E-05 0.800 1.000 30 1994 2016
Venous Thromboembolism
CUI: C1861172
Disease: Venous Thromboembolism
408 0.763 0.320 3 93905799 missense variant T/C snv 2.8E-05 1.4E-05 0.060 1.000 6 2014 2019
Deep Vein Thrombosis
CUI: C0149871
Disease: Deep Vein Thrombosis
93 0.763 0.320 3 93905799 missense variant T/C snv 2.8E-05 1.4E-05 0.030 1.000 3 2006 2010
Cerebral Infarction
CUI: C0007785
Disease: Cerebral Infarction
123 0.763 0.320 3 93905799 missense variant T/C snv 2.8E-05 1.4E-05 0.010 1.000 1 2015 2015
Factor V Leiden mutation
CUI: C0584960
Disease: Factor V Leiden mutation
46 0.763 0.320 3 93905799 missense variant T/C snv 2.8E-05 1.4E-05 0.010 1.000 1 2015 2015
Fetal Growth Retardation
CUI: C0015934
Disease: Fetal Growth Retardation
21 0.763 0.320 3 93905799 missense variant T/C snv 2.8E-05 1.4E-05 0.010 1.000 1 2014 2014
Malnutrition
CUI: C0162429
Disease: Malnutrition
29 0.763 0.320 3 93905799 missense variant T/C snv 2.8E-05 1.4E-05 0.010 1.000 1 2019 2019
Miscarriage
CUI: C4552766
Disease: Miscarriage
56 0.763 0.320 3 93905799 missense variant T/C snv 2.8E-05 1.4E-05 0.010 1.000 1 2014 2014
Thrombophilia, hereditary
CUI: C2584620
Disease: Thrombophilia, hereditary
9 0.763 0.320 3 93905799 missense variant T/C snv 2.8E-05 1.4E-05 0.010 1.000 1 2019 2019
Thrombosis of cerebral veins
CUI: C0151945
Disease: Thrombosis of cerebral veins
11 0.763 0.320 3 93905799 missense variant T/C snv 2.8E-05 1.4E-05 0.010 1.000 1 2019 2019
Vertical Talus
CUI: C0240912
Disease: Vertical Talus
20 0.763 0.320 3 93905799 missense variant T/C snv 2.8E-05 1.4E-05 0.010 1 2019 2019