rs60791294, ABCC6

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.
Pseudoxanthoma Elasticum
CUI: C0033847
Disease: Pseudoxanthoma Elasticum
323 0.882 0.280 16 16163086 missense variant C/G;T snv 7.6E-05 0.800 1.000 15 2000 2015
Abnormally lax or hyperextensible skin
CUI: C4024736
Disease: Abnormally lax or hyperextensible skin
53 0.882 0.280 16 16163086 missense variant C/G;T snv 7.6E-05 0.700 0
Angina Pectoris
CUI: C0002962
Disease: Angina Pectoris
65 0.882 0.280 16 16163086 missense variant C/G;T snv 7.6E-05 0.700 0
Angioid Streaks
CUI: C0002982
Disease: Angioid Streaks
90 0.882 0.280 16 16163086 missense variant C/G;T snv 7.6E-05 0.700 0
Cutaneous plaque
CUI: C0241148
Disease: Cutaneous plaque
107 0.882 0.280 16 16163086 missense variant C/G;T snv 7.6E-05 0.700 0
Electrocardiogram abnormal
CUI: C0522055
Disease: Electrocardiogram abnormal
54 0.882 0.280 16 16163086 missense variant C/G;T snv 7.6E-05 0.700 0
Gastrointestinal Hemorrhage
CUI: C0017181
Disease: Gastrointestinal Hemorrhage
24 0.882 0.280 16 16163086 missense variant C/G;T snv 7.6E-05 0.700 0
Intermittent Claudication
CUI: C0021775
Disease: Intermittent Claudication
69 0.882 0.280 16 16163086 missense variant C/G;T snv 7.6E-05 0.700 0
Nephrolithiasis
CUI: C0392525
Disease: Nephrolithiasis
99 0.882 0.280 16 16163086 missense variant C/G;T snv 7.6E-05 0.700 0
Papule
CUI: C0332563
Disease: Papule
131 0.882 0.280 16 16163086 missense variant C/G;T snv 7.6E-05 0.700 0
Retinal Hemorrhage
CUI: C0035317
Disease: Retinal Hemorrhage
86 0.882 0.280 16 16163086 missense variant C/G;T snv 7.6E-05 0.700 0