Human SNP ID | rs4668356 |
---|---|
Human chromosome | chr2 |
Human SNP position | 170965956 |
Pig chromosome | chr15 |
Pig SNP position | 86512722 |
PubMed ID | 19734545 |
---|---|
Journal | Hum Mol Genet |
Link | www.ncbi.nlm.nih.gov/pubmed/19734545 |
Study | A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB. |
Disease/Trait | Cognitive performance |
Initial sample | Up to 1,295 individuals |
Replication sample | NA |
Region | 2q31.1 |
Chromosome id | chr2 |
Chromosome position | 170965956 |
Reported gene | GORASP2 |
Mapped gene | GORASP2 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 26003 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs4668356-? |
SNPs | rs4668356 |
Merged | 0 |
SNP id current | 4668356 |
Context | synonymous_variant |
Intergenic | 0 |
Allele frequency | 0.06041 |
P value | 0.000001 |
Pvalue mlog | 6 |
P value text | (PAL8) |
Or beta | |
%95 Ci | |
Platform | Illumina [475971] |
CNV | N |
Mapped trait | neuropsychological test |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0003926 |
Study accession | GCST000477 |