Entrez Id: |
950 |
Gene Symbol: |
SCARB2 |
SCARB2
|
Epilepsy, Rolandic
|
0.100 |
CausalMutation |
CLINVAR |
Exome-wide analysis of mutational burden in patients with typical and atypical Rolandic epilepsy.
|
29358611 |
2018 |
Entrez Id: |
9681 |
Gene Symbol: |
DEPDC5 |
DEPDC5
|
Epilepsy, Rolandic
|
0.100 |
CausalMutation |
CLINVAR |
Exome-wide analysis of mutational burden in patients with typical and atypical Rolandic epilepsy.
|
29358611 |
2018 |
Entrez Id: |
1476 |
Gene Symbol: |
CSTB |
CSTB
|
Epilepsy, Rolandic
|
0.100 |
CausalMutation |
CLINVAR |
Exome-wide analysis of mutational burden in patients with typical and atypical Rolandic epilepsy.
|
29358611 |
2018 |
Entrez Id: |
7957 |
Gene Symbol: |
EPM2A |
EPM2A
|
Epilepsy, Rolandic
|
0.100 |
CausalMutation |
CLINVAR |
Exome-wide analysis of mutational burden in patients with typical and atypical Rolandic epilepsy.
|
29358611 |
2018 |
Entrez Id: |
5649 |
Gene Symbol: |
RELN |
RELN
|
Epilepsy, Rolandic
|
0.100 |
CausalMutation |
CLINVAR |
Exome-wide analysis of mutational burden in patients with typical and atypical Rolandic epilepsy.
|
29358611 |
2018 |
Entrez Id: |
2902 |
Gene Symbol: |
GRIN1 |
GRIN1
|
Epilepsy, Rolandic
|
0.100 |
CausalMutation |
CLINVAR |
Exome-wide analysis of mutational burden in patients with typical and atypical Rolandic epilepsy.
|
29358611 |
2018 |
SCN1A-AS1
|
Epilepsy, Rolandic
|
0.100 |
CausalMutation |
CLINVAR |
Exome-wide analysis of mutational burden in patients with typical and atypical Rolandic epilepsy.
|
29358611 |
2018 |
Entrez Id: |
102724428 |
Gene Symbol: |
SIK1B |
SIK1B
|
Epilepsy, Rolandic
|
0.100 |
CausalMutation |
CLINVAR |
Exome-wide analysis of mutational burden in patients with typical and atypical Rolandic epilepsy.
|
29358611 |
2018 |
Entrez Id: |
57582 |
Gene Symbol: |
KCNT1 |
KCNT1
|
Epilepsy, Rolandic
|
0.100 |
CausalMutation |
CLINVAR |
Exome-wide analysis of mutational burden in patients with typical and atypical Rolandic epilepsy.
|
29358611 |
2018 |
Entrez Id: |
26047 |
Gene Symbol: |
CNTNAP2 |
CNTNAP2
|
Epilepsy, Rolandic
|
0.100 |
CausalMutation |
CLINVAR |
Exome-wide analysis of mutational burden in patients with typical and atypical Rolandic epilepsy.
|
29358611 |
2018 |
Entrez Id: |
51124 |
Gene Symbol: |
IER3IP1 |
IER3IP1
|
Epilepsy, Rolandic
|
0.100 |
CausalMutation |
CLINVAR |
Exome-wide analysis of mutational burden in patients with typical and atypical Rolandic epilepsy.
|
29358611 |
2018 |
Entrez Id: |
79753 |
Gene Symbol: |
SNIP1 |
SNIP1
|
Epilepsy, Rolandic
|
0.100 |
CausalMutation |
CLINVAR |
Exome-wide analysis of mutational burden in patients with typical and atypical Rolandic epilepsy.
|
29358611 |
2018 |
Entrez Id: |
6529 |
Gene Symbol: |
SLC6A1 |
SLC6A1
|
Epilepsy, Rolandic
|
0.100 |
CausalMutation |
CLINVAR |
Exome-wide analysis of mutational burden in patients with typical and atypical Rolandic epilepsy.
|
29358611 |
2018 |
Entrez Id: |
92335 |
Gene Symbol: |
STRADA |
STRADA
|
Epilepsy, Rolandic
|
0.100 |
CausalMutation |
CLINVAR |
Exome-wide analysis of mutational burden in patients with typical and atypical Rolandic epilepsy.
|
29358611 |
2018 |
Entrez Id: |
57465 |
Gene Symbol: |
TBC1D24 |
TBC1D24
|
Epilepsy, Rolandic
|
0.100 |
CausalMutation |
CLINVAR |
Exome-wide analysis of mutational burden in patients with typical and atypical Rolandic epilepsy.
|
29358611 |
2018 |
Entrez Id: |
427 |
Gene Symbol: |
ASAH1 |
ASAH1
|
Epilepsy, Rolandic
|
0.100 |
CausalMutation |
CLINVAR |
Exome-wide analysis of mutational burden in patients with typical and atypical Rolandic epilepsy.
|
29358611 |
2018 |
Entrez Id: |
6513 |
Gene Symbol: |
SLC2A1 |
SLC2A1
|
Epilepsy, Rolandic
|
0.100 |
CausalMutation |
CLINVAR |
Exome-wide analysis of mutational burden in patients with typical and atypical Rolandic epilepsy.
|
29358611 |
2018 |
Entrez Id: |
6326 |
Gene Symbol: |
SCN2A |
SCN2A
|
Epilepsy, Rolandic
|
0.100 |
CausalMutation |
CLINVAR |
Exome-wide analysis of mutational burden in patients with typical and atypical Rolandic epilepsy.
|
29358611 |
2018 |
Entrez Id: |
1106 |
Gene Symbol: |
CHD2 |
CHD2
|
Epilepsy, Rolandic
|
0.100 |
CausalMutation |
CLINVAR |
Exome-wide analysis of mutational burden in patients with typical and atypical Rolandic epilepsy.
|
29358611 |
2018 |
PRICKLE2
|
Epilepsy, Rolandic
|
0.100 |
CausalMutation |
CLINVAR |
Exome-wide analysis of mutational burden in patients with typical and atypical Rolandic epilepsy.
|
29358611 |
2018 |
Entrez Id: |
6324 |
Gene Symbol: |
SCN1B |
SCN1B
|
Epilepsy, Rolandic
|
0.100 |
CausalMutation |
CLINVAR |
Exome-wide analysis of mutational burden in patients with typical and atypical Rolandic epilepsy.
|
29358611 |
2018 |
Entrez Id: |
57094 |
Gene Symbol: |
CPA6 |
CPA6
|
Epilepsy, Rolandic
|
0.100 |
CausalMutation |
CLINVAR |
Exome-wide analysis of mutational burden in patients with typical and atypical Rolandic epilepsy.
|
29358611 |
2018 |
Entrez Id: |
23236 |
Gene Symbol: |
PLCB1 |
PLCB1
|
Epilepsy, Rolandic
|
0.100 |
CausalMutation |
CLINVAR |
Exome-wide analysis of mutational burden in patients with typical and atypical Rolandic epilepsy.
|
29358611 |
2018 |
Entrez Id: |
57526 |
Gene Symbol: |
PCDH19 |
PCDH19
|
Epilepsy, Rolandic
|
0.100 |
CausalMutation |
CLINVAR |
Exome-wide analysis of mutational burden in patients with typical and atypical Rolandic epilepsy.
|
29358611 |
2018 |
Entrez Id: |
6709 |
Gene Symbol: |
SPTAN1 |
SPTAN1
|
Epilepsy, Rolandic
|
0.100 |
CausalMutation |
CLINVAR |
Exome-wide analysis of mutational burden in patients with typical and atypical Rolandic epilepsy.
|
29358611 |
2018 |