SNP Detail For rs478597
1.Mapping Information
Human SNP ID rs478597
Human chromosome chr12
Human SNP position 117313620
Pig chromosome chr14
Pig SNP position 37440135
2.Annotation Information
PubMed ID18821565
JournalAm J Med Genet B Neuropsychiatr Genet
Linkwww.ncbi.nlm.nih.gov/pubmed/18821565
StudyGenome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations.
Disease/TraitInattentive symptoms
Initial sample930 European ancestry trios
Replication sampleNA
Region12q24.22
Chromosome idchr12
Chromosome position117313620
Reported geneintergenic
Mapped geneNOS1
Upstream gene id
Downstream gene id
SNP gene ids4842
Upstream gene distance
Downstream gene distance
SNP risk allelers478597-?
SNPsrs478597
Merged0
SNP id current478597
Contextintron_variant
Intergenic0
Allele frequencyNR
P value0.000008
Pvalue mlog5.09691001300805
P value text(binary)
Or beta
%95 Ci
PlatformPerlegen [429981]
CNVN
Mapped traitbehavior
Mapped trait URIhttp://purl.obolibrary.org/obo/GO_0007610
Study accessionGCST000279