SNP Detail For rs7236632
1.Mapping Information
Human SNP ID rs7236632
Human chromosome chr18
Human SNP position 57766970
Pig chromosome chr1
Pig SNP position 180583568
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
Region18q21.31
Chromosome idchr18
Chromosome position57766970
Reported geneATP8B1
Mapped geneLOC105376870, ATP8B1
Upstream gene id
Downstream gene id
SNP gene ids105376870, 5205
Upstream gene distance
Downstream gene distance
SNP risk allelers7236632-A
SNPsrs7236632
Merged0
SNP id current7236632
Contextintron_variant
Intergenic0
Allele frequency0.86
P value0.000006
Pvalue mlog5.22184874961635
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