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rs12059546

From SNPedia

Orientationplus
Stabilizedplus
Make rs12059546(A;A)
Make rs12059546(A;G)
Make rs12059546(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position239806797
GeneCHRM3
is asnp
is mentioned by
dbSNPrs12059546
ebirs12059546
HLIrs12059546
Exacrs12059546
Varsomers12059546
Maprs12059546
PheGenIrs12059546
hapmaprs12059546
1000 genomesrs12059546
hgdprs12059546
ensemblrs12059546
gopubmedrs12059546
geneviewrs12059546
scholarrs12059546
googlers12059546
pharmgkbrs12059546
gwascentralrs12059546
openSNPrs12059546
23andMers12059546
23andMe allrs12059546
SNP Nexus

SNPshotrs12059546
SNPdbers12059546
MSV3drs12059546
GWAS Ctlgrs12059546
GMAF0.3205
Max Magnitude
? (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]