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rs2184898

From SNPedia

Orientationplus
Stabilizedplus
Make rs2184898(A;A)
Make rs2184898(A;G)
Make rs2184898(G;G)
ReferenceGRCh38 38.1/142
Chromosome10
Position117658593
is asnp
is mentioned by
dbSNPrs2184898
ebirs2184898
HLIrs2184898
Exacrs2184898
Varsomers2184898
Maprs2184898
PheGenIrs2184898
hapmaprs2184898
1000 genomesrs2184898
hgdprs2184898
ensemblrs2184898
gopubmedrs2184898
geneviewrs2184898
scholarrs2184898
googlers2184898
pharmgkbrs2184898
gwascentralrs2184898
openSNPrs2184898
23andMers2184898
23andMe allrs2184898
SNP Nexus

SNPshotrs2184898
SNPdbers2184898
MSV3drs2184898
GWAS Ctlgrs2184898
GMAF0.2732
Max Magnitude
? (A;A) (A;G) (G;G) 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 1.33 [1.18-1.50]