Human SNP ID | rs4658552 |
---|---|
Human chromosome | chr1 |
Human SNP position | 243249634 |
Pig chromosome | chr10 |
Pig SNP position | 18531578 |
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 | 1q43 |
Chromosome id | chr1 |
Chromosome position | 243249634 |
Reported gene | SDCCAG8, AKT3 |
Mapped gene | CEP170 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 9859 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs4658552-T |
SNPs | rs4658552 |
Merged | 0 |
SNP id current | 4658552 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | 0.632 |
P value | 0.000002 |
Pvalue mlog | 5.69897000433601 |
P value text | |
Or beta | 0.021 |
%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 |