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rs13398848

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs13398848(A;G)
Make rs13398848(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position84018044
is asnp
is mentioned by
dbSNPrs13398848
ebirs13398848
HLIrs13398848
Exacrs13398848
Varsomers13398848
Maprs13398848
PheGenIrs13398848
hapmaprs13398848
1000 genomesrs13398848
hgdprs13398848
ensemblrs13398848
gopubmedrs13398848
geneviewrs13398848
scholarrs13398848
googlers13398848
pharmgkbrs13398848
gwascentralrs13398848
openSNPrs13398848
23andMers13398848
23andMe allrs13398848
SNP Nexus

SNPshotrs13398848
SNPdbers13398848
MSV3drs13398848
GWAS Ctlgrs13398848
GMAF0.08219
Max Magnitude0
? (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 0.000005
Odds Ratio 1.59 [1.30-1.95]