rs12059546
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs12059546(A;A) |
Make rs12059546(A;G) |
Make rs12059546(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 239806797 |
Gene | CHRM3 |
is a | snp |
is | mentioned by |
dbSNP | rs12059546 |
dbSNP (classic) | rs12059546 |
ClinGen | rs12059546 |
ebi | rs12059546 |
HLI | rs12059546 |
Exac | rs12059546 |
Gnomad | rs12059546 |
Varsome | rs12059546 |
LitVar | rs12059546 |
Map | rs12059546 |
PheGenI | rs12059546 |
Biobank | rs12059546 |
1000 genomes | rs12059546 |
hgdp | rs12059546 |
ensembl | rs12059546 |
geneview | rs12059546 |
scholar | rs12059546 |
rs12059546 | |
pharmgkb | rs12059546 |
gwascentral | rs12059546 |
openSNP | rs12059546 |
23andMe | rs12059546 |
SNPshot | rs12059546 |
SNPdbe | rs12059546 |
MSV3d | rs12059546 |
GWAS Ctlg | rs12059546 |
GMAF | 0.3205 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 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 | G |
P-val | 4E-8 |
Odds Ratio | 1.42 [1.26-1.61] |