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rs11890028

From SNPedia

Orientationplus
Stabilizedplus
Make rs11890028(G;G)
Make rs11890028(G;T)
Make rs11890028(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position166086767
GeneSCN1A
is asnp
is mentioned by
dbSNPrs11890028
ebirs11890028
HLIrs11890028
Exacrs11890028
Varsomers11890028
Maprs11890028
PheGenIrs11890028
hapmaprs11890028
1000 genomesrs11890028
hgdprs11890028
ensemblrs11890028
gopubmedrs11890028
geneviewrs11890028
scholarrs11890028
googlers11890028
pharmgkbrs11890028
gwascentralrs11890028
openSNPrs11890028
23andMers11890028
23andMe allrs11890028
SNP Nexus

SNPshotrs11890028
SNPdbers11890028
MSV3drs11890028
GWAS Ctlgrs11890028
GMAF0.1974
Max Magnitude
? (G;G) (G;T) (T;T) 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 T
P-val 4E-6
Odds Ratio 1.18 [1.09-1.27]