rs567798234, AMPD2

N. diseases: 5
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.
Congestive heart failure
CUI: C0018802
Disease: Congestive heart failure
165 0.851 0.120 1 109625326 missense variant C/T snv 4.1E-06 7.0E-06 0.010 1.000 1 2014 2014
Glycogen Storage Disease Type V
CUI: C0017924
Disease: Glycogen Storage Disease Type V
76 0.851 0.120 1 109625326 missense variant C/T snv 4.1E-06 7.0E-06 0.010 1.000 1 2008 2008
Heart failure
CUI: C0018801
Disease: Heart failure
201 0.851 0.120 1 109625326 missense variant C/T snv 4.1E-06 7.0E-06 0.010 1.000 1 2014 2014
Myocardial Ischemia
CUI: C0151744
Disease: Myocardial Ischemia
103 0.851 0.120 1 109625326 missense variant C/T snv 4.1E-06 7.0E-06 0.010 1.000 1 2014 2014
Ventilatory Threshold
CUI: C4086945
Disease: Ventilatory Threshold
1 0.851 0.120 1 109625326 missense variant C/T snv 4.1E-06 7.0E-06 0.010 1.000 1 2008 2008