Source: CLINVAR ×
Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
CUI: C3151464
Disease: ATRIAL FIBRILLATION, FAMILIAL, 10
ATRIAL FIBRILLATION, FAMILIAL, 10 		1 0 1 0.33 0 0
CUI: C3502809
Disease: Generalized Epilepsy with Febrile Seizures Plus
Generalized Epilepsy with Febrile Seizures Plus 		1 0 1 0.33 0 0
CUI: C3809311
Disease: ATRIAL FIBRILLATION, FAMILIAL, 13
ATRIAL FIBRILLATION, FAMILIAL, 13 		1 0 1 0.33 0 0
CUI: C4016241
Disease: HUTCHINSON-GILFORD PROGERIA SYNDROME, ATYPICAL
HUTCHINSON-GILFORD PROGERIA SYNDROME, ATYPICAL 		1 0 1 0.33 0 0
CUI: C4016652
Disease: ATRIAL STANDSTILL 1, DIGENIC
ATRIAL STANDSTILL 1, DIGENIC 		1 0 1 0.33 0 0
CUI: C4229131
Disease: Distal acroosteolysis
Distal acroosteolysis 		1 0 1 0.33 0 0
CUI: C4479236
Disease: EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 52
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 52 		1 0 1 0.33 0 0
CUI: C4551804
Disease: Brugada Syndrome 1
Brugada Syndrome 1 		1 34 1 0.33 1 2.7E-02
CUI: C0002962
Disease: Angina Pectoris
Angina Pectoris 		2 0 1 0.25 0 0
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation 		2 0 1 0.25 0 0
CUI: C0023787
Disease: Lipodystrophy
Lipodystrophy 		2 0 1 0.25 0 0
CUI: C0038644
Disease: Sudden infant death syndrome
Sudden infant death syndrome 		2 0 1 0.25 0 0
CUI: C0406585
Disease: Lethal tight skin contracture syndrome (disorder)
Lethal tight skin contracture syndrome (disorder) 		2 0 1 0.25 0 0
CUI: C1879286
Disease: Hereditary bundle branch system defect
Hereditary bundle branch system defect 		2 0 1 0.25 0 0
CUI: C3276240
Disease: LONG QT SYNDROME 2/3, DIGENIC
LONG QT SYNDROME 2/3, DIGENIC 		2 0 1 0.25 0 0
CUI: C3276241
Disease: LONG QT SYNDROME 3/6, DIGENIC Disorder
LONG QT SYNDROME 3/6, DIGENIC Disorder 		2 0 1 0.25 0 0
CUI: C4021779
Disease: Abnormality of the calf musculature
Abnormality of the calf musculature 		2 0 1 0.25 0 0
CUI: C4022012
Disease: Death in early adulthood
Death in early adulthood 		2 0 1 0.25 0 0
CUI: C1960469
Disease: Left ventricular noncompaction
Left ventricular noncompaction 		8 0 2 0.22 0 0
CUI: C0162298
Disease: Joint stiffness
Joint stiffness 		3 0 1 0.20 0 0
CUI: C0340493
Disease: Paroxysmal familial ventricular fibrillation
Paroxysmal familial ventricular fibrillation 		3 0 1 0.20 0 0
CUI: C1142166
Disease: Brugada Syndrome (disorder)
Brugada Syndrome (disorder) 		3 103 1 0.20 1 9.4E-03
CUI: C1843392
Disease: Death in childhood
Death in childhood 		3 0 1 0.20 0 0
CUI: C1854154
Disease: Charcot-Marie-Tooth disease, Type 2B1
Charcot-Marie-Tooth disease, Type 2B1 		3 0 1 0.20 0 0
CUI: C0340427
Disease: Familial dilated cardiomyopathy
Familial dilated cardiomyopathy 		10 0 2 0.18 0 0