|
OMIM |
Link |
Information gain |
01 |
|
ARVD3
|
[NCBI]
|
0.00102023
|
|
|
CPVT
|
[NCBI]
|
0.000886515
|
|
|
RYR2
|
[NCBI]
|
0.000815017
|
|
|
CASQ2
|
[NCBI]
|
0.000550804
|
|
|
andersen cardiodysrhythmic periodic paralysis
|
[NCBI]
|
0.000240509
|
|
|
ventricular tachycardia, familial
|
[NCBI]
|
0.00023291
|
|
|
GJA1
|
[NCBI]
|
0.000142602
|
|
|
apnea, obstructive sleep
|
[NCBI]
|
0.000142159
|
|
|
FKBP1B
|
[NCBI]
|
0.000122892
|
|
|
KCNH2
|
[NCBI]
|
0.000108758
|
|
|
cardiac arrhythmia, ankyrin-b-related
|
[NCBI]
|
9.51693e-05
|
|
|
LVNCX
|
[NCBI]
|
9.1078e-05
|
|
|
VF
|
[NCBI]
|
9.1078e-05
|
|
|
LVNC1
|
[NCBI]
|
9.1078e-05
|
|
|
cardiomyopathy, dilated, with woolly hair and keratoderma
|
[NCBI]
|
8.78187e-05
|
|
|
ARVD2
|
[NCBI]
|
8.78187e-05
|
|
|
SQT1
|
[NCBI]
|
8.5109e-05
|
|
|
cardiac conduction defect
|
[NCBI]
|
8.279e-05
|
|
|
KCNIP2
|
[NCBI]
|
8.21209e-05
|
|
|
gitelman syndrome
|
[NCBI]
|
7.73439e-05
|
|
|
SP4
|
[NCBI]
|
6.83427e-05
|
|
|
ARVD1
|
[NCBI]
|
6.65411e-05
|
|
|
brugada syndrome 1
|
[NCBI]
|
6.57736e-05
|
|
|
GNAI2
|
[NCBI]
|
5.97685e-05
|
|
|
MCOPS7
|
[NCBI]
|
5.91268e-05
|
|
|
ANK2
|
[NCBI]
|
5.72593e-05
|
|
|
DM2
|
[NCBI]
|
5.14471e-05
|
|
|
ADRB1
|
[NCBI]
|
4.98282e-05
|
|
|
CLS
|
[NCBI]
|
4.81669e-05
|
|
|
GJA5
|
[NCBI]
|
4.63428e-05
|
|
|
SLC25A20
|
[NCBI]
|
4.43549e-05
|
|
|
CMH
|
[NCBI]
|
3.47368e-05
|
|
|
SCN5A
|
[NCBI]
|
3.31275e-05
|
|
|
KCNQ1
|
[NCBI]
|
3.31275e-05
|
|
|
RYR1
|
[NCBI]
|
3.07725e-05
|
|
|
dystrophia myotonica 1
|
[NCBI]
|
2.80488e-05
|
|
|
NGFB
|
[NCBI]
|
2.48659e-05
|
|
|
PD
|
[NCBI]
|
1.01421e-05
|
|
|
NPPA
|
[NCBI]
|
7.0761e-06
|
|
|
EPO
|
[NCBI]
|
1.17994e-06
|
|