rs11861787
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs11861787(A;A) |
Make rs11861787(A;C) |
Make rs11861787(C;C) |
Reference | GRCh38 38.1/142 |
Chromosome | 16 |
Position | 8467743 |
is a | snp |
is | mentioned by |
dbSNP | rs11861787 |
dbSNP (classic) | rs11861787 |
ClinGen | rs11861787 |
ebi | rs11861787 |
HLI | rs11861787 |
Exac | rs11861787 |
Gnomad | rs11861787 |
Varsome | rs11861787 |
LitVar | rs11861787 |
Map | rs11861787 |
PheGenI | rs11861787 |
Biobank | rs11861787 |
1000 genomes | rs11861787 |
hgdp | rs11861787 |
ensembl | rs11861787 |
geneview | rs11861787 |
scholar | rs11861787 |
rs11861787 | |
pharmgkb | rs11861787 |
gwascentral | rs11861787 |
openSNP | rs11861787 |
23andMe | rs11861787 |
SNPshot | rs11861787 |
SNPdbe | rs11861787 |
MSV3d | rs11861787 |
GWAS Ctlg | rs11861787 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 23962720] |
Trait | Epilepsy (remission after treatment) |
Title | A genome-wide association study and biological pathway analysis of epilepsy prognosis in a prospective cohort of newly treated epilepsy. |
Risk Allele | C |
P-val | 3E-6 |
Odds Ratio | 1.89 [NR] |