SNP Detail For rs1256531
1.Mapping Information
Human SNP ID rs1256531
Human chromosome chr14
Human SNP position 65281041
Pig chromosome chr2
Pig SNP position 78361872
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 (symptom count)
Initial sample872 European, African American and other ancestry substance dependence cases, 3,091 European, African American and other ancestry controls
Replication sampleNA
Region14q23.3
Chromosome idchr14
Chromosome position65281041
Reported geneintergenic
Mapped geneLOC105370536, PTBP1P
Upstream gene id
Downstream gene id
SNP gene ids105370536, 122888
Upstream gene distance
Downstream gene distance
SNP risk allelers1256531-G
SNPsrs1256531
Merged0
SNP id current1256531
Contextnon_coding_transcript_exon_variant
Intergenic0
Allele frequency0.234
P value0.000004
Pvalue mlog5.39794000867203
P value text
Or beta0.09
%95 Ci[NR] unit increase
PlatformIllumina [948658]
CNVN
Mapped traitconduct disorder
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0004216
Study accessionGCST000713