rs63751001, ABCC6

N. diseases: 13
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.
Angina Pectoris
CUI: C0002962
Disease: Angina Pectoris
65 0.790 0.240 16 16159555 missense variant C/T snv 2.8E-05 0.700 0
Angioid Streaks
CUI: C0002982
Disease: Angioid Streaks
90 0.790 0.240 16 16159555 missense variant C/T snv 2.8E-05 0.700 0
ARTERIAL CALCIFICATION, GENERALIZED, OF INFANCY, 2
CUI: C3276161
Disease: ARTERIAL CALCIFICATION, GENERALIZED, OF INFANCY, 2
16 0.790 0.240 16 16159555 missense variant C/T snv 2.8E-05 0.700 0
Cutaneous plaque
CUI: C0241148
Disease: Cutaneous plaque
107 0.790 0.240 16 16159555 missense variant C/T snv 2.8E-05 0.700 0
Electrocardiogram abnormal
CUI: C0522055
Disease: Electrocardiogram abnormal
54 0.790 0.240 16 16159555 missense variant C/T snv 2.8E-05 0.700 0
Intermittent Claudication
CUI: C0021775
Disease: Intermittent Claudication
69 0.790 0.240 16 16159555 missense variant C/T snv 2.8E-05 0.700 0
Papule
CUI: C0332563
Disease: Papule
131 0.790 0.240 16 16159555 missense variant C/T snv 2.8E-05 0.700 0
Pseudoxanthoma Elasticum
CUI: C0033847
Disease: Pseudoxanthoma Elasticum
323 0.790 0.240 16 16159555 missense variant C/T snv 2.8E-05 0.700 0
Retinal Hemorrhage
CUI: C0035317
Disease: Retinal Hemorrhage
86 0.790 0.240 16 16159555 missense variant C/T snv 2.8E-05 0.700 0
Acute myocardial infarction
CUI: C0155626
Disease: Acute myocardial infarction
118 0.790 0.240 16 16159555 missense variant C/T snv 2.8E-05 0.010 1.000 1 2007 2007
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.790 0.240 16 16159555 missense variant C/T snv 2.8E-05 0.010 1.000 1 2007 2007
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.790 0.240 16 16159555 missense variant C/T snv 2.8E-05 0.010 1.000 1 2007 2007
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.790 0.240 16 16159555 missense variant C/T snv 2.8E-05 0.010 1.000 1 2007 2007