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rs2717068

From SNPedia

Orientationminus
Stabilizedminus
Make rs2717068(G;G)
Make rs2717068(G;T)
Make rs2717068(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position57867738
is asnp
is mentioned by
dbSNPrs2717068
ebirs2717068
HLIrs2717068
Exacrs2717068
Varsomers2717068
Maprs2717068
PheGenIrs2717068
hapmaprs2717068
1000 genomesrs2717068
hgdprs2717068
ensemblrs2717068
gopubmedrs2717068
geneviewrs2717068
scholarrs2717068
googlers2717068
pharmgkbrs2717068
gwascentralrs2717068
openSNPrs2717068
23andMers2717068
23andMe allrs2717068
SNP Nexus

SNPshotrs2717068
SNPdbers2717068
MSV3drs2717068
GWAS Ctlgrs2717068
GMAF0.2916
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-7
Odds Ratio 1.27 [1.16-1.40]