Human SNP ID | rs2392362 |
---|---|
Human chromosome | chr7 |
Human SNP position | 35361837 |
Pig chromosome | chr18 |
Pig SNP position | 42362188 |
PubMed ID | 21130836 |
---|---|
Journal | Biol Psychol |
Link | www.ncbi.nlm.nih.gov/pubmed/21130836 |
Study | Whole genome association scan for genetic polymorphisms influencing information processing speed. |
Disease/Trait | Information processing speed |
Initial sample | Up to 4,039 European ancestry individuals |
Replication sample | NA |
Region | 7p14.2 |
Chromosome id | chr7 |
Chromosome position | 35361837 |
Reported gene | AC007652.1 |
Mapped gene | LOC401324 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 401324 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs2392362-T |
SNPs | rs2392362 |
Merged | 0 |
SNP id current | 2392362 |
Context | intergenic_variant |
Intergenic | 0 |
Allele frequency | 0.27 |
P value | 0.000002 |
Pvalue mlog | 5.69897000433601 |
P value text | (inspection time) |
Or beta | 0.14 |
%95 Ci | [0.08-0.20] unit increase |
Platform | Illumina [~ 610000] |
CNV | N |
Mapped trait | information processing speed |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0004363 |
Study accession | GCST000905 |