rs2717068
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs2717068(G;G) |
Make rs2717068(G;T) |
Make rs2717068(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 57867738 |
is a | snp |
is | mentioned by |
dbSNP | rs2717068 |
dbSNP (classic) | rs2717068 |
ClinGen | rs2717068 |
ebi | rs2717068 |
HLI | rs2717068 |
Exac | rs2717068 |
Gnomad | rs2717068 |
Varsome | rs2717068 |
LitVar | rs2717068 |
Map | rs2717068 |
PheGenI | rs2717068 |
Biobank | rs2717068 |
1000 genomes | rs2717068 |
hgdp | rs2717068 |
ensembl | rs2717068 |
geneview | rs2717068 |
scholar | rs2717068 |
rs2717068 | |
pharmgkb | rs2717068 |
gwascentral | rs2717068 |
openSNP | rs2717068 |
23andMe | rs2717068 |
SNPshot | rs2717068 |
SNPdbe | rs2717068 |
MSV3d | rs2717068 |
GWAS Ctlg | rs2717068 |
GMAF | 0.2916 |
Max Magnitude | 0 |
? | (G;G) (G;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 22949513] |
Trait | Epilepsy (generalized) |
Title | Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32 |
Risk Allele | T |
P-val | 4E-7 |
Odds Ratio | 1.27 [1.16-1.40] |