Human SNP ID | rs11947645 |
---|---|
Human chromosome | chr4 |
Human SNP position | 150180520 |
Pig chromosome | chr8 |
Pig SNP position | 83633055 |
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 | 4q31.23 |
Chromosome id | chr4 |
Chromosome position | 150180520 |
Reported gene | DCLK2 |
Mapped gene | DCLK2 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 166614 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs11947645-A |
SNPs | rs11947645 |
Merged | 0 |
SNP id current | 11947645 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | |
P value | 0.000001 |
Pvalue mlog | 6 |
P value text | |
Or beta | 5.329 |
%95 Ci | [3.17-7.48] 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 |