rs61670327
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs61670327(A;A) |
Make rs61670327(A;G) |
Make rs61670327(G;G) |
Reference | GRCh38 38.1/142 |
Chromosome | 5 |
Position | 3276582 |
is a | snp |
is | mentioned by |
dbSNP | rs61670327 |
dbSNP (classic) | rs61670327 |
ClinGen | rs61670327 |
ebi | rs61670327 |
HLI | rs61670327 |
Exac | rs61670327 |
Gnomad | rs61670327 |
Varsome | rs61670327 |
LitVar | rs61670327 |
Map | rs61670327 |
PheGenI | rs61670327 |
Biobank | rs61670327 |
1000 genomes | rs61670327 |
hgdp | rs61670327 |
ensembl | rs61670327 |
geneview | rs61670327 |
scholar | rs61670327 |
rs61670327 | |
pharmgkb | rs61670327 |
gwascentral | rs61670327 |
openSNP | rs61670327 |
23andMe | rs61670327 |
SNPshot | rs61670327 |
SNPdbe | rs61670327 |
MSV3d | rs61670327 |
GWAS Ctlg | rs61670327 |
Max Magnitude | 0 |
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 | A |
P-val | 7E-7 |
Odds Ratio | 1.72 [NR] |