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rs7950811

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs7950811(A;A)
Make rs7950811(A;C)
ReferenceGRCh38 38.1/141
Chromosome11
Position92917836
GeneMIR194-2
is asnp
is mentioned by
dbSNPrs7950811
ebirs7950811
HLIrs7950811
Exacrs7950811
Varsomers7950811
Maprs7950811
PheGenIrs7950811
hapmaprs7950811
1000 genomesrs7950811
hgdprs7950811
ensemblrs7950811
gopubmedrs7950811
geneviewrs7950811
scholarrs7950811
googlers7950811
pharmgkbrs7950811
gwascentralrs7950811
openSNPrs7950811
23andMers7950811
23andMe allrs7950811
SNP Nexus

SNPshotrs7950811
SNPdbers7950811
MSV3drs7950811
GWAS Ctlgrs7950811
GMAF0.08494
Max Magnitude0
? (A;A) (A;C) (C;C) 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 9E-7
Odds Ratio 1.65 [1.35-2.00]