|
OMIM |
Link |
Information gain |
01 |
|
creatinine clearance quantitative trait locus
|
[NCBI]
|
0.00254657
|
|
|
red cell phospholipid defect with hemolysis
|
[NCBI]
|
0.0015281
|
|
|
GAMT
|
[NCBI]
|
0.00112819
|
|
|
IGAN1
|
[NCBI]
|
0.00100259
|
|
|
EKD1
|
[NCBI]
|
0.00077906
|
|
|
creatine deficiency syndrome, x-linked
|
[NCBI]
|
0.000640618
|
|
|
MAFD6
|
[NCBI]
|
0.000621821
|
|
|
SLC6A8
|
[NCBI]
|
0.000424702
|
|
|
VWM
|
[NCBI]
|
0.000275695
|
|
|
MDD
|
[NCBI]
|
0.000190749
|
|
|
AD
|
[NCBI]
|
0.000176326
|
|
|
CKBE
|
[NCBI]
|
0.000151659
|
|
|
ALD
|
[NCBI]
|
0.000137455
|
|
|
GATM
|
[NCBI]
|
0.000102455
|
|
|
charcot-marie-tooth disease and deafness
|
[NCBI]
|
0.000100488
|
|
|
myasthenia, limb-girdle, familial
|
[NCBI]
|
9.47597e-05
|
|
|
PTH
|
[NCBI]
|
9.02132e-05
|
|
|
EIG
|
[NCBI]
|
8.80633e-05
|
|
|
TS
|
[NCBI]
|
8.36962e-05
|
|
|
CF
|
[NCBI]
|
8.30927e-05
|
|
|
PD
|
[NCBI]
|
7.87075e-05
|
|
|
renal cysts and diabetes syndrome
|
[NCBI]
|
7.78414e-05
|
|
|
KSS
|
[NCBI]
|
7.62804e-05
|
|
|
alexander disease
|
[NCBI]
|
6.99451e-05
|
|
|
NPHP1
|
[NCBI]
|
6.6854e-05
|
|
|
FHM1
|
[NCBI]
|
6.41459e-05
|
|
|
hyperornithinemia-hyperammonemia-homocitrullinuria syndrome
|
[NCBI]
|
6.17377e-05
|
|
|
central core disease of muscle
|
[NCBI]
|
5.76017e-05
|
|
|
myoclonic epilepsy of unverricht and lundborg
|
[NCBI]
|
4.85502e-05
|
|
|
ARPKD
|
[NCBI]
|
4.85502e-05
|
|
|
vitamin d-dependent rickets, type ii
|
[NCBI]
|
4.272e-05
|
|
|
SLS
|
[NCBI]
|
3.89508e-05
|
|
|
ornithine aminotransferase deficiency
|
[NCBI]
|
3.86829e-05
|
|
|
FTD
|
[NCBI]
|
3.69704e-05
|
|
|
RA
|
[NCBI]
|
3.31341e-05
|
|
|
UCP3
|
[NCBI]
|
3.17059e-05
|
|
|
FFI
|
[NCBI]
|
2.88302e-05
|
|
|
AHO
|
[NCBI]
|
2.83905e-05
|
|
|
DRPLA
|
[NCBI]
|
2.63434e-05
|
|
|
SMAX1
|
[NCBI]
|
2.48646e-05
|
|
|
PMD
|
[NCBI]
|
2.35056e-05
|
|
|
EIF2B5
|
[NCBI]
|
2.26749e-05
|
|
|
SLC22A8
|
[NCBI]
|
2.03088e-05
|
|
|
HNF1B
|
[NCBI]
|
1.93186e-05
|
|
|
dystrophia myotonica 1
|
[NCBI]
|
1.78201e-05
|
|
|
ASPA
|
[NCBI]
|
1.63142e-05
|
|
|
SLC6A6
|
[NCBI]
|
1.58306e-05
|
|
|
HD
|
[NCBI]
|
1.50224e-05
|
|
|
GFAP
|
[NCBI]
|
1.34896e-05
|
|
|
ASL
|
[NCBI]
|
1.34696e-05
|
|
|
APOD
|
[NCBI]
|
1.31873e-05
|
|
|
EGF
|
[NCBI]
|
1.24505e-05
|
|
|
GPT
|
[NCBI]
|
1.23084e-05
|
|
|
ASS
|
[NCBI]
|
1.11817e-05
|
|
|
FRAP1
|
[NCBI]
|
1.05882e-05
|
|
|
PG
|
[NCBI]
|
1.01188e-05
|
|
|
NPPA
|
[NCBI]
|
8.40449e-06
|
|
|
EPO
|
[NCBI]
|
7.53493e-06
|
|
|
CAT
|
[NCBI]
|
7.4223e-06
|
|
|
ABP1
|
[NCBI]
|
7.42087e-06
|
|
|
SOD1
|
[NCBI]
|
6.5122e-06
|
|
|
MAP2
|
[NCBI]
|
6.24348e-06
|
|
|
ADM
|
[NCBI]
|
5.93442e-06
|
|
|
VDR
|
[NCBI]
|
5.22189e-06
|
|
|
SLE
|
[NCBI]
|
4.60247e-06
|
|
|
MPO
|
[NCBI]
|
4.43267e-06
|
|
|
PRL
|
[NCBI]
|
4.19368e-06
|
|
|
MB
|
[NCBI]
|
3.71872e-06
|
|
|
CTGF
|
[NCBI]
|
3.48347e-06
|
|
|
PF4
|
[NCBI]
|
3.41349e-06
|
|
|
panencephalitis, subacute sclerosing
|
[NCBI]
|
2.51707e-06
|
|
|
MG
|
[NCBI]
|
2.3539e-06
|
|
|
lymphoma, non-hodgkin, familial
|
[NCBI]
|
2.17978e-06
|
|
|
TNF
|
[NCBI]
|
2.13693e-06
|
|
|
NPY
|
[NCBI]
|
2.11422e-06
|
|
|
TTR
|
[NCBI]
|
2.10495e-06
|
|
|
TNFRSF11B
|
[NCBI]
|
1.88869e-06
|
|
|
GAPDH
|
[NCBI]
|
1.78834e-06
|
|
|
APOE
|
[NCBI]
|
1.61799e-06
|
|
|
SHBG
|
[NCBI]
|
1.30531e-06
|
|
|
AVP
|
[NCBI]
|
1.16475e-06
|
|
|
TH
|
[NCBI]
|
1.00363e-06
|
|
|
PCNA
|
[NCBI]
|
7.40143e-07
|
|
|
G6PD
|
[NCBI]
|
7.04918e-07
|
|
|
BDNF
|
[NCBI]
|
2.59099e-07
|
|
|
CJD
|
[NCBI]
|
7.12028e-08
|
|
|
ACHE
|
[NCBI]
|
1.05135e-08
|
|
|
CHAT
|
[NCBI]
|
6.5542e-09
|
|