Rs10776612

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Orientationplus
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ReferenceGRCh37 37.1/131
Chromosome10
Position49735563
GeneARHGAP22
is asnp
is mentioned by
dbSNPrs10776612
Exacrs10776612
PheGenIrs10776612
nextbiors10776612
hapmaprs10776612
1000 genomesrs10776612
hgdprs10776612
ensemblrs10776612
gopubmedrs10776612
geneviewrs10776612
scholarrs10776612
googlers10776612
pharmgkbrs10776612
gwascentralrs10776612
openSNPrs10776612
23andMers10776612
23andMe allrs10776612
SNP Nexus

SNPshotrs10776612
SNPdbers10776612
MSV3drs10776612
GMAF0.4536
? (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 0.000002
Odds Ratio 1.33 [1.18-1.49]