rs2292096
|
|
|
0.810 |
GeneticVariation |
BEFREE |
Here, we report that rs2292096 genotypes tended to associate with expression of CAMSAP1L1 RNA in the temporal lobe (p=0.054) and hippocampus (p=0.20) of epilepsy surgery patients, with expression tending to increase with the G allele.
|
24148305 |
2013 |
rs2292096
|
|
|
0.810 |
GeneticVariation |
GWASDB |
Two-stage genome-wide association study identifies variants in CAMSAP1L1 as susceptibility loci for epilepsy in Chinese.
|
22116939 |
2012 |
rs2292096
|
|
|
0.810 |
GeneticVariation |
GWASCAT |
Two-stage genome-wide association study identifies variants in CAMSAP1L1 as susceptibility loci for epilepsy in Chinese.
|
22116939 |
2012 |
rs10030601
|
|
C |
0.800 |
GeneticVariation |
GWASCAT |
Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32.
|
22949513 |
2012 |
rs10030601
|
|
C |
0.800 |
GeneticVariation |
GWASDB |
Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32.
|
22949513 |
2012 |
rs10496964
|
|
C |
0.800 |
GeneticVariation |
GWASDB |
Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32.
|
22949513 |
2012 |
rs10496964
|
|
C |
0.800 |
GeneticVariation |
GWASCAT |
Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32.
|
22949513 |
2012 |
rs12059546
|
|
G |
0.800 |
GeneticVariation |
GWASCAT |
Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32.
|
22949513 |
2012 |
rs12059546
|
|
G |
0.800 |
GeneticVariation |
GWASDB |
Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32.
|
22949513 |
2012 |
rs13026414
|
|
C |
0.800 |
GeneticVariation |
GWASDB |
Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32.
|
22949513 |
2012 |
rs13026414
|
|
C |
0.800 |
GeneticVariation |
GWASCAT |
Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32.
|
22949513 |
2012 |
rs2717068
|
|
T |
0.800 |
GeneticVariation |
GWASDB |
Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32.
|
22949513 |
2012 |
rs2717068
|
|
T |
0.800 |
GeneticVariation |
GWASCAT |
Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32.
|
22949513 |
2012 |
rs39861
|
|
C |
0.800 |
GeneticVariation |
GWASCAT |
Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32.
|
22949513 |
2012 |
rs39861
|
|
C |
0.800 |
GeneticVariation |
GWASDB |
Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32.
|
22949513 |
2012 |
rs72823592
|
|
G |
0.800 |
GeneticVariation |
GWASCAT |
Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32.
|
22949513 |
2012 |
rs72823592
|
|
G |
0.800 |
GeneticVariation |
GWASDB |
Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32.
|
22949513 |
2012 |
rs771390
|
|
C |
0.800 |
GeneticVariation |
GWASCAT |
Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32.
|
22949513 |
2012 |
rs771390
|
|
C |
0.800 |
GeneticVariation |
GWASDB |
Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32.
|
22949513 |
2012 |
rs1558005340
|
|
G |
0.700 |
GeneticVariation |
CLINVAR |
Biallelic loss of function variants in ATP1A2 cause hydrops fetalis, microcephaly, arthrogryposis and extensive cortical malformations.
|
30690204 |
2020 |
rs1558008455
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Biallelic loss of function variants in ATP1A2 cause hydrops fetalis, microcephaly, arthrogryposis and extensive cortical malformations.
|
30690204 |
2020 |
rs111908689
|
|
|
0.700 |
GeneticVariation |
GWASCAT |
A genome-wide association study of sodium levels and drug metabolism in an epilepsy cohort treated with carbamazepine and oxcarbazepine.
|
30868120 |
2019 |
rs11214136
|
|
|
0.700 |
GeneticVariation |
GWASCAT |
A genome-wide association study of sodium levels and drug metabolism in an epilepsy cohort treated with carbamazepine and oxcarbazepine.
|
30868120 |
2019 |
rs1394074
|
|
|
0.700 |
GeneticVariation |
GWASCAT |
A genome-wide association study of sodium levels and drug metabolism in an epilepsy cohort treated with carbamazepine and oxcarbazepine.
|
30868120 |
2019 |
rs148173957
|
|
|
0.700 |
GeneticVariation |
GWASCAT |
A genome-wide association study of sodium levels and drug metabolism in an epilepsy cohort treated with carbamazepine and oxcarbazepine.
|
30868120 |
2019 |