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rs4434872

From SNPedia

Orientationplus
Stabilizedplus
Make rs4434872(C;C)
Make rs4434872(C;T)
Make rs4434872(T;T)
ReferenceGRCh37.p5 37.3/137
Chromosome1
Position153774276
GeneWDR5B
is asnp
is mentioned by
dbSNPrs4434872
ebirs4434872
HLIrs4434872
Exacrs4434872
Varsomers4434872
Maprs4434872
PheGenIrs4434872
hapmaprs4434872
1000 genomesrs4434872
hgdprs4434872
ensemblrs4434872
gopubmedrs4434872
geneviewrs4434872
scholarrs4434872
googlers4434872
pharmgkbrs4434872
gwascentralrs4434872
openSNPrs4434872
23andMers4434872
23andMe allrs4434872
SNP Nexus

SNPshotrs4434872
SNPdbers4434872
MSV3drs4434872
GWAS Ctlgrs4434872
GMAF0.3411
Max Magnitude
? (C;C) (C;T) (T;T) 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 0.000008
Odds Ratio 0.08 [NR] unit increase


[PMID 18505370OA-icon.png] Identification of a linkage disequilibrium block in chromosome 1q associated with BMD in premenopausal white women.