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rs72823592

From SNPedia

Orientationplus
Stabilizedplus
Make rs72823592(A;A)
Make rs72823592(A;G)
Make rs72823592(G;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position48045642
GeneLOC102724556
is asnp
is mentioned by
dbSNPrs72823592
ebirs72823592
HLIrs72823592
Exacrs72823592
Varsomers72823592
Maprs72823592
PheGenIrs72823592
hapmaprs72823592
1000 genomesrs72823592
hgdprs72823592
ensemblrs72823592
gopubmedrs72823592
geneviewrs72823592
scholarrs72823592
googlers72823592
pharmgkbrs72823592
gwascentralrs72823592
openSNPrs72823592
23andMers72823592
23andMe allrs72823592
SNP Nexus

SNPshotrs72823592
SNPdbers72823592
MSV3drs72823592
GWAS Ctlgrs72823592
GMAF0.129
Max Magnitude
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 G
P-val 9E-9
Odds Ratio 1.30 [1.20-1.41]