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rs771390

From SNPedia

Orientationplus
Stabilizedplus
Make rs771390(C;C)
Make rs771390(C;T)
Make rs771390(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position34285335
is asnp
is mentioned by
dbSNPrs771390
ClinGenrs771390
ebirs771390
HLIrs771390
Exacrs771390
Varsomers771390
Maprs771390
PheGenIrs771390
hapmaprs771390
1000 genomesrs771390
hgdprs771390
ensemblrs771390
gopubmedrs771390
geneviewrs771390
scholarrs771390
googlers771390
pharmgkbrs771390
gwascentralrs771390
openSNPrs771390
23andMers771390
23andMe allrs771390
SNP Nexus

SNPshotrs771390
SNPdbers771390
MSV3drs771390
GWAS Ctlgrs771390
GMAF0.1648
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 6E-7
Odds Ratio 1.22 [1.12-1.32]