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rs11861787

From SNPedia

Orientationplus
Stabilizedplus
Make rs11861787(A;A)
Make rs11861787(A;C)
Make rs11861787(C;C)
ReferenceGRCh38 38.1/142
Chromosome16
Position8467743
is asnp
is mentioned by
dbSNPrs11861787
ebirs11861787
HLIrs11861787
Exacrs11861787
Varsomers11861787
Maprs11861787
PheGenIrs11861787
hapmaprs11861787
1000 genomesrs11861787
hgdprs11861787
ensemblrs11861787
gopubmedrs11861787
geneviewrs11861787
scholarrs11861787
googlers11861787
pharmgkbrs11861787
gwascentralrs11861787
openSNPrs11861787
23andMers11861787
23andMe allrs11861787
SNP Nexus

SNPshotrs11861787
SNPdbers11861787
MSV3drs11861787
GWAS Ctlgrs11861787
Max Magnitude
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 23962720OA-icon.png]
Trait Epilepsy (remission after treatment)
Title A genome-wide association study and biological pathway analysis of epilepsy prognosis in a prospective cohort of newly treated epilepsy.
Risk Allele C
P-val 3E-6
Odds Ratio 1.89 [NR]