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rs10496964

From SNPedia

Orientationplus
Stabilizedplus
Make rs10496964(C;C)
Make rs10496964(C;T)
Make rs10496964(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position144602342
is asnp
is mentioned by
dbSNPrs10496964
ebirs10496964
HLIrs10496964
Exacrs10496964
Varsomers10496964
Maprs10496964
PheGenIrs10496964
hapmaprs10496964
1000 genomesrs10496964
hgdprs10496964
ensemblrs10496964
gopubmedrs10496964
geneviewrs10496964
scholarrs10496964
googlers10496964
pharmgkbrs10496964
gwascentralrs10496964
openSNPrs10496964
23andMers10496964
23andMe allrs10496964
SNP Nexus

SNPshotrs10496964
SNPdbers10496964
MSV3drs10496964
GWAS Ctlgrs10496964
GMAF0.124
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 9E-9
Odds Ratio 1.47 [1.28-1.67]