SNP Detail For rs4434872
1.Mapping Information
Human SNP ID rs4434872
Human chromosome chr1
Human SNP position 153801800
Pig chromosome chr4
Pig SNP position 104770528
2.Annotation Information
PubMed ID20585324
JournalMol Psychiatry
Linkwww.ncbi.nlm.nih.gov/pubmed/20585324
StudyGenome-wide association study of conduct disorder symptomatology.
Disease/TraitConduct disorder (symptom count)
Initial sample872 European, African American and other ancestry substance dependence cases, 3,091 European, African American and other ancestry controls
Replication sampleNA
Region1q21.3
Chromosome idchr1
Chromosome position153801800
Reported geneLOC343052
Mapped geneLOC105371448
Upstream gene id
Downstream gene id
SNP gene ids105371448
Upstream gene distance
Downstream gene distance
SNP risk allelers4434872-T
SNPsrs4434872
Merged0
SNP id current4434872
Contextsplice_region_variant
Intergenic0
Allele frequency0.263
P value0.000008
Pvalue mlog5.09691001300805
P value text
Or beta0.08
%95 Ci[NR] unit increase
PlatformIllumina [948658]
CNVN
Mapped traitconduct disorder
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0004216
Study accessionGCST000713