Human SNP ID | rs10444533 |
---|---|
Human chromosome | chr12 |
Human SNP position | 106835927 |
Pig chromosome | chr5 |
Pig SNP position | 13381510 |
PubMed ID | 24133439 |
---|---|
Journal | Front Hum Neurosci |
Link | www.ncbi.nlm.nih.gov/pubmed/24133439 |
Study | Genome-wide association study of autistic-like traits in a general population study of young adults. |
Disease/Trait | Social autistic-like traits |
Initial sample | 965 European ancestry young adult individuals |
Replication sample | NA |
Region | 12q23.3 |
Chromosome id | chr12 |
Chromosome position | 106835927 |
Reported gene | RIC8B |
Mapped gene | RIC8B |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 55188 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs10444533-C |
SNPs | rs10444533 |
Merged | 0 |
SNP id current | 10444533 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | |
P value | 0.000004 |
Pvalue mlog | 5.39794000867203 |
P value text | |
Or beta | 1.458 |
%95 Ci | [0.84-2.07] unit increase |
Platform | Illumina [2462046] (imputed) |
CNV | N |
Mapped trait | autism spectrum disorder symptom |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0005426 |
Study accession | GCST002228 |