Human SNP ID | rs710865 |
---|---|
Human chromosome | chr1 |
Human SNP position | 19242478 |
Pig chromosome | chr6 |
Pig SNP position | 71803953 |
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 | 1p36.13 |
Chromosome id | chr1 |
Chromosome position | 19242478 |
Reported gene | KIAA0090, MRT04, AKR7L |
Mapped gene | EMC1 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 23065 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs710865-? |
SNPs | rs710865 |
Merged | 0 |
SNP id current | 710865 |
Context | splice_region_variant |
Intergenic | 0 |
Allele frequency | 0.38 |
P value | 0.0000001 |
Pvalue mlog | 7 |
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 |