Human SNP ID | rs1970584 |
---|---|
Human chromosome | chr9 |
Human SNP position | 123348027 |
Pig chromosome | chr1 |
Pig SNP position | 297917065 |
PubMed ID | 25201988 |
---|---|
Journal | Proc Natl Acad Sci U S A |
Link | www.ncbi.nlm.nih.gov/pubmed/25201988 |
Study | Common genetic variants associated with cognitive performance identified using the proxy-phenotype method. |
Disease/Trait | Educational attainment |
Initial sample | 106,736 European ancestry individuals |
Replication sample | NA |
Region | 9q33.3 |
Chromosome id | chr9 |
Chromosome position | 123348027 |
Reported gene | intergenic |
Mapped gene | LOC105376265 - CRB2 |
Upstream gene id | 105376265 |
Downstream gene id | 286204 |
SNP gene ids | |
Upstream gene distance | 25417 |
Downstream gene distance | 6432 |
SNP risk allele | rs1970584-A |
SNPs | rs1970584 |
Merged | 0 |
SNP id current | 1970584 |
Context | intergenic_variant |
Intergenic | 1 |
Allele frequency | 0.06 |
P value | 0.0000005 |
Pvalue mlog | 6.30102999566398 |
P value text | |
Or beta | 0.048 |
%95 Ci | [NR] unit increase |
Platform | Affymetrix, Illumina [NR] (imputed) |
CNV | N |
Mapped trait | self reported educational attainment |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0004784 |
Study accession | GCST002598 |