rs150821281, PKP2

N. diseases: 7
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.
Arrhythmogenic Right Ventricular Dysplasia
CUI: C0349788
Disease: Arrhythmogenic Right Ventricular Dysplasia
136 0.827 0.080 12 32878461 missense variant G/A snv 2.3E-03 2.5E-03 0.010 1 2016 2016
Cardiac Arrhythmia
CUI: C0003811
Disease: Cardiac Arrhythmia
111 0.827 0.080 12 32878461 missense variant G/A snv 2.3E-03 2.5E-03 0.010 1.000 1 2016 2016
Cardiomyopathy, Dilated
CUI: C0007193
Disease: Cardiomyopathy, Dilated
509 0.827 0.080 12 32878461 missense variant G/A snv 2.3E-03 2.5E-03 0.010 1.000 1 2016 2016
Cardiomyopathy, Familial Idiopathic
CUI: C1449563
Disease: Cardiomyopathy, Familial Idiopathic
243 0.827 0.080 12 32878461 missense variant G/A snv 2.3E-03 2.5E-03 0.010 1.000 1 2016 2016
Congestive heart failure
CUI: C0018802
Disease: Congestive heart failure
165 0.827 0.080 12 32878461 missense variant G/A snv 2.3E-03 2.5E-03 0.010 1 2016 2016
Heart failure
CUI: C0018801
Disease: Heart failure
201 0.827 0.080 12 32878461 missense variant G/A snv 2.3E-03 2.5E-03 0.010 1 2016 2016
Hypertrophic Cardiomyopathy
CUI: C0007194
Disease: Hypertrophic Cardiomyopathy
635 0.827 0.080 12 32878461 missense variant G/A snv 2.3E-03 2.5E-03 0.010 1 2016 2016