Human SNP ID | rs490592 |
---|---|
Human chromosome | chr11 |
Human SNP position | 116427650 |
Pig chromosome | chr9 |
Pig SNP position | 48861280 |
PubMed ID | 20171287 |
---|---|
Journal | Neuroimage |
Link | www.ncbi.nlm.nih.gov/pubmed/20171287 |
Study | Voxelwise genome-wide association study (vGWAS). |
Disease/Trait | Brain structure |
Initial sample | 740 European ancestry individuals |
Replication sample | NA |
Region | 11q23.3 |
Chromosome id | chr11 |
Chromosome position | 116427650 |
Reported gene | intergenic |
Mapped gene | LOC105369513 - LOC101929011 |
Upstream gene id | 105369513 |
Downstream gene id | 101929011 |
SNP gene ids | |
Upstream gene distance | 346594 |
Downstream gene distance | 211772 |
SNP risk allele | rs490592-? |
SNPs | rs490592 |
Merged | 0 |
SNP id current | 490592 |
Context | intergenic_variant |
Intergenic | 1 |
Allele frequency | 0.21 |
P value | 0.000001 |
Pvalue mlog | 6 |
P value text | |
Or beta | |
%95 Ci | |
Platform | Illumina [448293] |
CNV | N |
Mapped trait | brain measurement |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0004464 |
Study accession | GCST000597 |