|
OMIM |
Link |
Information gain |
01 |
|
PFHB1B
|
[NCBI]
|
0.00412986
|
|
|
PFHB2
|
[NCBI]
|
0.00200072
|
|
|
bundle branch block, familial isolated complete right
|
[NCBI]
|
0.00119841
|
|
|
PFHB1A
|
[NCBI]
|
0.000944651
|
|
|
brugada syndrome 1
|
[NCBI]
|
0.000590684
|
|
|
SCN5A
|
[NCBI]
|
0.0003552
|
|
|
KSS
|
[NCBI]
|
0.000158043
|
|
|
ARVD1
|
[NCBI]
|
0.000156886
|
|
|
acrocephalopolysyndactyly type iii
|
[NCBI]
|
0.000131618
|
|
|
myoclonic epilepsy, congenital deafness, macular dystrophy, and psychiatric disorders
|
[NCBI]
|
0.000131618
|
|
|
DM2
|
[NCBI]
|
0.000126042
|
|
|
brugada syndrome 2
|
[NCBI]
|
0.000100673
|
|
|
GPD1L
|
[NCBI]
|
8.05705e-05
|
|
|
GJA5
|
[NCBI]
|
6.37462e-05
|
|
|
CMH
|
[NCBI]
|
3.47368e-05
|
|
|
RA
|
[NCBI]
|
3.28911e-05
|
|