SNP Detail For rs1557488
1.Mapping Information
Human SNP ID rs1557488
Human chromosome chr11
Human SNP position 126749295
Pig chromosome chr9
Pig SNP position 59703231
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
Region11q24.2
Chromosome idchr11
Chromosome position126749295
Reported geneKIRREL3
Mapped geneKIRREL3
Upstream gene id
Downstream gene id
SNP gene ids84623
Upstream gene distance
Downstream gene distance
SNP risk allelers1557488-T
SNPsrs1557488
Merged0
SNP id current1557488
Contextintron_variant
Intergenic0
Allele frequency0.18
P value0.000005
Pvalue mlog5.30102999566398
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