Human SNP ID | rs10500871 |
---|---|
Human chromosome | chr11 |
Human SNP position | 20194210 |
Pig chromosome | chr2 |
Pig SNP position | 42156363 |
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 | 11p15.1 |
Chromosome id | chr11 |
Chromosome position | 20194210 |
Reported gene | intergenic |
Mapped gene | LOC105376583 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 105376583 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs10500871-T |
SNPs | rs10500871 |
Merged | 0 |
SNP id current | 10500871 |
Context | intergenic_variant |
Intergenic | 0 |
Allele frequency | 0.322 |
P value | 0.000003 |
Pvalue mlog | 5.52287874528033 |
P value text | |
Or beta | 0.022 |
%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 |