rs7587026
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs7587026(A;A) |
Make rs7587026(A;C) |
Make rs7587026(C;C) |
Reference | GRCh38 38.1/142 |
Chromosome | 2 |
Position | 166122240 |
Gene | LOC101929680, SCN1A |
is a | snp |
is | mentioned by |
dbSNP | rs7587026 |
dbSNP (classic) | rs7587026 |
ClinGen | rs7587026 |
ebi | rs7587026 |
HLI | rs7587026 |
Exac | rs7587026 |
Gnomad | rs7587026 |
Varsome | rs7587026 |
LitVar | rs7587026 |
Map | rs7587026 |
PheGenI | rs7587026 |
Biobank | rs7587026 |
1000 genomes | rs7587026 |
hgdp | rs7587026 |
ensembl | rs7587026 |
geneview | rs7587026 |
scholar | rs7587026 |
rs7587026 | |
pharmgkb | rs7587026 |
gwascentral | rs7587026 |
openSNP | rs7587026 |
23andMe | rs7587026 |
SNPshot | rs7587026 |
SNPdbe | rs7587026 |
MSV3d | rs7587026 |
GWAS Ctlg | rs7587026 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 24014518] |
Trait | Mesial temporal lobe epilepsy with hippocampal sclerosis |
Title | Epilepsy, hippocampal sclerosis and febrile seizures linked by common genetic variation around SCN1A. |
Risk Allele | A |
P-val | 4E-8 |
Odds Ratio | 1.24 [1.15-1.34] |