Human SNP ID | rs9036 |
---|---|
Human chromosome | chr3 |
Human SNP position | 14489213 |
Pig chromosome | chr13 |
Pig SNP position | 77609905 |
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 | 3p25.1 |
Chromosome id | chr3 |
Chromosome position | 14489213 |
Reported gene | GRIP2 |
Mapped gene | GRIP2, SLC6A6 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 80852, 6533 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs9036-? |
SNPs | rs9036 |
Merged | 0 |
SNP id current | 9036 |
Context | 3_prime_UTR_variant |
Intergenic | 0 |
Allele frequency | 0.187 |
P value | 0.000003 |
Pvalue mlog | 5.52287874528033 |
P value text | (PAL6) |
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 |