Human SNP ID | rs448720 |
---|---|
Human chromosome | chr15 |
Human SNP position | 67906573 |
Pig chromosome | chr1 |
Pig SNP position | 183596482 |
PubMed ID | 20125193 |
---|---|
Journal | Eur J Hum Genet |
Link | www.ncbi.nlm.nih.gov/pubmed/20125193 |
Study | Common genetic variation and performance on standardized cognitive tests. |
Disease/Trait | Cognitive performance |
Initial sample | Up to 813 European ancestry individuals, up to 167 East Asian ancestry individuals, up to 7 Hispanic/Latin American individuals, up to 74 South Asian ancestry individuals |
Replication sample | NA |
Region | 15q23 |
Chromosome id | chr15 |
Chromosome position | 67906573 |
Reported gene | RNU6-2, RNU6-1 |
Mapped gene | RNU6-1 - PIAS1 |
Upstream gene id | 26827 |
Downstream gene id | 8554 |
SNP gene ids | |
Upstream gene distance | 66528 |
Downstream gene distance | 147661 |
SNP risk allele | rs448720-? |
SNPs | rs448720 |
Merged | 0 |
SNP id current | 448720 |
Context | intergenic_variant |
Intergenic | 1 |
Allele frequency | NR |
P value | 0.000005 |
Pvalue mlog | 5.30102999566398 |
P value text | (TrailsB) |
Or beta | |
%95 Ci | |
Platform | Illumina [up to 563855] |
CNV | N |
Mapped trait | neuropsychological test |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0003926 |
Study accession | GCST000579 |