rs1063856, VWF

N. diseases: 14
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.
Coagulation factor measurement
CUI: C1167912
Disease: Coagulation factor measurement
26 0.763 0.400 12 6044368 missense variant T/C;G snv 0.31 0.700 1.000 1 2013 2013
Factor VII measurement
CUI: C2825856
Disease: Factor VII measurement
36 0.763 0.400 12 6044368 missense variant T/C;G snv 0.31 0.700 1.000 1 2013 2013
Factor VIII measurement
CUI: C2825857
Disease: Factor VIII measurement
42 0.763 0.400 12 6044368 missense variant T/C;G snv 0.31 0.700 1.000 1 2010 2010
Diabetes Mellitus, Non-Insulin-Dependent
2672 0.763 0.400 12 6044368 missense variant T/C;G snv 0.31 0.020 0.500 2 2003 2005
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.763 0.400 12 6044368 missense variant T/C;G snv 0.31 0.010 1.000 1 2005 2005
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.763 0.400 12 6044368 missense variant T/C;G snv 0.31 0.010 1.000 1 2005 2005
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.763 0.400 12 6044368 missense variant T/C;G snv 0.31 0.010 1 2005 2005
Diabetes
CUI: C0011847
Disease: Diabetes
710 0.763 0.400 12 6044368 missense variant T/C;G snv 0.31 0.010 1.000 1 2000 2000
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
824 0.763 0.400 12 6044368 missense variant T/C;G snv 0.31 0.010 1.000 1 2000 2000
Diabetes Mellitus, Insulin-Dependent
954 0.763 0.400 12 6044368 missense variant T/C;G snv 0.31 0.010 1.000 1 2000 2000
Kidney Diseases
CUI: C0022658
Disease: Kidney Diseases
140 0.763 0.400 12 6044368 missense variant T/C;G snv 0.31 0.010 1.000 1 2000 2000
PIGMENTARY DISORDER, RETICULATE, WITH SYSTEMIC MANIFESTATIONS
37 0.763 0.400 12 6044368 missense variant T/C;G snv 0.31 0.010 1.000 1 2003 2003
Sleep Apnea, Obstructive
CUI: C0520679
Disease: Sleep Apnea, Obstructive
105 0.763 0.400 12 6044368 missense variant T/C;G snv 0.31 0.010 1.000 1 2019 2019
von Willebrand Disease, Type 3
CUI: C1264041
Disease: von Willebrand Disease, Type 3
17 0.763 0.400 12 6044368 missense variant T/C;G snv 0.31 0.010 1.000 1 2014 2014