Human SNP ID | rs889956 |
---|---|
Human chromosome | chr2 |
Human SNP position | 57177699 |
Pig chromosome | chr3 |
Pig SNP position | 88894876 |
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 | 2p16.1 |
Chromosome id | chr2 |
Chromosome position | 57177699 |
Reported gene | intergenic |
Mapped gene | LOC101927213 - LOC105377632 |
Upstream gene id | 101927213 |
Downstream gene id | 105377632 |
SNP gene ids | |
Upstream gene distance | 581786 |
Downstream gene distance | 112177 |
SNP risk allele | rs889956-A |
SNPs | rs889956 |
Merged | 0 |
SNP id current | 889956 |
Context | intergenic_variant |
Intergenic | 1 |
Allele frequency | 0.397 |
P value | 0.0000002 |
Pvalue mlog | 6.69897000433601 |
P value text | |
Or beta | 0.023 |
%95 Ci | [NR] unit decrease |
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 |