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rs11838918

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs11838918(C;C)
Make rs11838918(C;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position78836439
GeneLINC00331
is asnp
is mentioned by
dbSNPrs11838918
ebirs11838918
HLIrs11838918
Exacrs11838918
Varsomers11838918
Maprs11838918
PheGenIrs11838918
hapmaprs11838918
1000 genomesrs11838918
hgdprs11838918
ensemblrs11838918
gopubmedrs11838918
geneviewrs11838918
scholarrs11838918
googlers11838918
pharmgkbrs11838918
gwascentralrs11838918
openSNPrs11838918
23andMers11838918
23andMe allrs11838918
SNP Nexus

SNPshotrs11838918
SNPdbers11838918
MSV3drs11838918
GWAS Ctlgrs11838918
GMAF0.01607
Max Magnitude0
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 20585324OA-icon.png]
Trait Conduct disorder (case status)
Title Genome-wide association study of conduct disorder symptomatology
Risk Allele
P-val 0.000003
Odds Ratio 2.26 [1.61-3.18]