SNP Detail For rs10831284
1.Mapping Information
Human SNP ID rs10831284
Human chromosome chr11
Human SNP position 94934799
Pig chromosome chr9
Pig SNP position 30767465
2.Annotation Information
PubMed ID18951430
JournalAm J Med Genet B Neuropsychiatr Genet
Linkwww.ncbi.nlm.nih.gov/pubmed/18951430
StudyConduct disorder and ADHD: evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study.
Disease/TraitAttention deficit hyperactivity disorder and conduct disorder
Initial sample938 European ancestry trios
Replication sampleNA
Region11q21
Chromosome idchr11
Chromosome position94934799
Reported geneAMOTL1, CWC15, JMJD2D
Mapped geneAMOTL1 - CWC15
Upstream gene id154810
Downstream gene id51503
SNP gene ids
Upstream gene distance58046
Downstream gene distance27823
SNP risk allelers10831284-G
SNPsrs10831284
Merged0
SNP id current10831284
Contextregulatory_region_variant
Intergenic1
Allele frequency0.13
P value0.000002
Pvalue mlog5.69897000433601
P value text
Or beta
%95 Ci
PlatformPerlegen [378332]
CNVN
Mapped traitattention deficit hyperactivity disorder, conduct disorder
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0003888, http://www.ebi.ac.uk/efo/EFO_0004216
Study accessionGCST000253