Human SNP ID | rs17750321 |
---|---|
Human chromosome | chr18 |
Human SNP position | 37498719 |
Pig chromosome | chr6 |
Pig SNP position | 114126072 |
PubMed ID | 24564958 |
---|---|
Journal | Mol Autism |
Link | www.ncbi.nlm.nih.gov/pubmed/24564958 |
Study | Variability in the common genetic architecture of social-communication spectrum phenotypes during childhood and adolescence. |
Disease/Trait | Social communication problems |
Initial sample | Up to 5,628 European ancestry individuals |
Replication sample | NA |
Region | 18q12.2 |
Chromosome id | chr18 |
Chromosome position | 37498719 |
Reported gene | BRUNOL4 |
Mapped gene | CELF4 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 56853 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs17750321-A |
SNPs | rs17750321 |
Merged | 0 |
SNP id current | 17750321 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | 0.03 |
P value | 0.000005 |
Pvalue mlog | 5.30102999566398 |
P value text | (Age 8) |
Or beta | 0.3 |
%95 Ci | [0.18-0.42] unit increase |
Platform | Illumina [2293137] (imputed) |
CNV | N |
Mapped trait | social communication impairment |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0005427 |
Study accession | GCST002367 |