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rs2122554

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in complete genomics
(G;G) 0
Make rs2122554(A;A)
Make rs2122554(A;C)
ReferenceGRCh38 38.1/141
Chromosome5
Position166530081
is asnp
is mentioned by
dbSNPrs2122554
ebirs2122554
HLIrs2122554
Exacrs2122554
Varsomers2122554
Maprs2122554
PheGenIrs2122554
hapmaprs2122554
1000 genomesrs2122554
hgdprs2122554
ensemblrs2122554
gopubmedrs2122554
geneviewrs2122554
scholarrs2122554
googlers2122554
pharmgkbrs2122554
gwascentralrs2122554
openSNPrs2122554
23andMers2122554
23andMe allrs2122554
SNP Nexus

SNPshotrs2122554
SNPdbers2122554
MSV3drs2122554
GWAS Ctlgrs2122554
GMAF0.1997
Max Magnitude0
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 20585324OA-icon.png]
Trait Conduct disorder (symptom count)
Title Genome-wide association study of conduct disorder symptomatology
Risk Allele
P-val 0.000003
Odds Ratio 0.10 [NR] unit decrease