SNP Detail For rs8179116
1.Mapping Information
Human SNP ID rs8179116
Human chromosome chr12
Human SNP position 108631651
Pig chromosome chr14
Pig SNP position 44712176
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
Region12q24.11
Chromosome idchr12
Chromosome position108631651
Reported geneSELPLG
Mapped geneLOC105369968, SELPLG
Upstream gene id
Downstream gene id
SNP gene ids105369968, 6404
Upstream gene distance
Downstream gene distance
SNP risk allelers8179116-A
SNPsrs8179116
Merged0
SNP id current8179116
Contextintron_variant
Intergenic0
Allele frequency0.021
P value0.000003
Pvalue mlog5.52287874528033
P value text
Or beta0.23
%95 Ci[NR] unit increase
PlatformIllumina [948658]
CNVN
Mapped traitconduct disorder
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0004216
Study accessionGCST000713