Human SNP ID | rs12125971 |
---|---|
Human chromosome | chr1 |
Human SNP position | 106921021 |
Pig chromosome | chr4 |
Pig SNP position | 123600093 |
PubMed ID | 22449649 |
---|---|
Journal | J Am Acad Child Adolesc Psychiatry |
Link | www.ncbi.nlm.nih.gov/pubmed/22449649 |
Study | Genome-wide association study of intelligence: additive effects of novel brain expressed genes. |
Disease/Trait | Intelligence |
Initial sample | 656 European ancestry individuals from ADHD families |
Replication sample | NA |
Region | 1p13.3 |
Chromosome id | chr1 |
Chromosome position | 106921021 |
Reported gene | PRMT6 |
Mapped gene | LOC105378889 - PRMT6 |
Upstream gene id | 105378889 |
Downstream gene id | 55170 |
SNP gene ids | |
Upstream gene distance | 42719 |
Downstream gene distance | 135624 |
SNP risk allele | rs12125971-? |
SNPs | rs12125971 |
Merged | 0 |
SNP id current | 12125971 |
Context | intergenic_variant |
Intergenic | 1 |
Allele frequency | NR |
P value | 0.000007 |
Pvalue mlog | 5.15490195998574 |
P value text | (High intelligence) |
Or beta | 6.93 |
%95 Ci | [3.99-9.87] unit increase |
Platform | Illumina [795637] |
CNV | N |
Mapped trait | intelligence |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0004337 |
Study accession | GCST001428 |