Have questions? Visit https://www.reddit.com/r/SNPedia

rs13026414

From SNPedia

Orientationplus
Stabilizedplus
Make rs13026414(C;C)
Make rs13026414(C;T)
Make rs13026414(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position57706920
GeneLOC101927235
is asnp
is mentioned by
dbSNPrs13026414
ebirs13026414
HLIrs13026414
Exacrs13026414
Varsomers13026414
Maprs13026414
PheGenIrs13026414
hapmaprs13026414
1000 genomesrs13026414
hgdprs13026414
ensemblrs13026414
gopubmedrs13026414
geneviewrs13026414
scholarrs13026414
googlers13026414
pharmgkbrs13026414
gwascentralrs13026414
openSNPrs13026414
23andMers13026414
23andMe allrs13026414
SNP Nexus

SNPshotrs13026414
SNPdbers13026414
MSV3drs13026414
GWAS Ctlgrs13026414
GMAF0.2612
Max Magnitude
? (C;C) (C;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 C
P-val 2E-9
Odds Ratio 1.23 [1.15-1.32]