Human SNP ID | rs1867503 |
---|---|
Human chromosome | chr3 |
Human SNP position | 133691804 |
Pig chromosome | chr13 |
Pig SNP position | 82375280 |
PubMed ID | 25534755 |
---|---|
Journal | Biol Psychiatry |
Link | www.ncbi.nlm.nih.gov/pubmed/25534755 |
Study | A Genome-wide Association Study of Autism Using the Simons Simplex Collection: Does Reducing Phenotypic Heterogeneity in Autism Increase Genetic Homogeneity? |
Disease/Trait | Autism spectrum disorder-related traits |
Initial sample | 1633 European ancestry trios, 942 trios |
Replication sample | NA |
Region | 3q22.1 |
Chromosome id | chr3 |
Chromosome position | 133691804 |
Reported gene | intergenic |
Mapped gene | TF |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 7018 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs1867503-? |
SNPs | rs1867503 |
Merged | 0 |
SNP id current | 1867503 |
Context | non_coding_transcript_exon_variant |
Intergenic | 0 |
Allele frequency | NR |
P value | 0.0000004 |
Pvalue mlog | 6.39794000867203 |
P value text | (ASD paternal model) |
Or beta | 1.55 |
%95 Ci | [1.30-1.84] |
Platform | Illumina [up to 2017939] |
CNV | N |
Mapped trait | autism spectrum disorder |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0003756 |
Study accession | GCST002639 |