Human SNP ID | rs2073233 |
---|---|
Human chromosome | chr20 |
Human SNP position | 12893937 |
Pig chromosome | chr17 |
Pig SNP position | 24273331 |
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 | 20p12.1 |
Chromosome id | chr20 |
Chromosome position | 12893937 |
Reported gene | intergenic |
Mapped gene | LOC101929486 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 101929486 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs2073233-? |
SNPs | rs2073233 |
Merged | 0 |
SNP id current | 2073233 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | 0.43 |
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 |