SNP Detail For rs1867503
1.Mapping Information
Human SNP ID rs1867503
Human chromosome chr3
Human SNP position 133691804
Pig chromosome chr13
Pig SNP position 82375280
2.Annotation Information
PubMed ID25534755
JournalBiol Psychiatry
Linkwww.ncbi.nlm.nih.gov/pubmed/25534755
StudyA Genome-wide Association Study of Autism Using the Simons Simplex Collection: Does Reducing Phenotypic Heterogeneity in Autism Increase Genetic Homogeneity?
Disease/TraitAutism spectrum disorder-related traits
Initial sample1633 European ancestry trios, 942 trios
Replication sampleNA
Region3q22.1
Chromosome idchr3
Chromosome position133691804
Reported geneintergenic
Mapped geneTF
Upstream gene id
Downstream gene id
SNP gene ids7018
Upstream gene distance
Downstream gene distance
SNP risk allelers1867503-?
SNPsrs1867503
Merged0
SNP id current1867503
Contextnon_coding_transcript_exon_variant
Intergenic0
Allele frequencyNR
P value0.0000004
Pvalue mlog6.39794000867203
P value text(ASD paternal model)
Or beta1.55
%95 Ci[1.30-1.84]
PlatformIllumina [up to 2017939]
CNVN
Mapped traitautism spectrum disorder
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0003756
Study accessionGCST002639