SNP Detail For rs2184898
1.Mapping Information
Human SNP ID rs2184898
Human chromosome chr10
Human SNP position 117658593
Pig chromosome chr14
Pig SNP position 139152386
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
Initial sample872 European, African American and other ancestry substance dependence cases, 3,091 European, African American and other ancestry controls
Replication sampleNA
Region10q26.11
Chromosome idchr10
Chromosome position117658593
Reported geneintergenic
Mapped geneEMX2 - LOC102724627
Upstream gene id2018
Downstream gene id102724627
SNP gene ids
Upstream gene distance109047
Downstream gene distance76341
SNP risk allelers2184898-A
SNPsrs2184898
Merged0
SNP id current2184898
Contextintergenic_variant
Intergenic1
Allele frequency0.327
P value0.000003
Pvalue mlog5.52287874528033
P value text
Or beta1.33
%95 Ci[1.18-1.50]
PlatformIllumina [948658]
CNVN
Mapped traitconduct disorder
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0004216
Study accessionGCST000714