Human SNP ID | rs2970992 |
---|---|
Human chromosome | chr2 |
Human SNP position | 100705847 |
Pig chromosome | chr3 |
Pig SNP position | 56143193 |
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 | 2q11.2 |
Chromosome id | chr2 |
Chromosome position | 100705847 |
Reported gene | NPAS2, NMS |
Mapped gene | NANOGNBP1 - LOC105373508 |
Upstream gene id | 100859926 |
Downstream gene id | 105373508 |
SNP gene ids | |
Upstream gene distance | 44903 |
Downstream gene distance | 34100 |
SNP risk allele | rs2970992-A |
SNPs | rs2970992 |
Merged | 0 |
SNP id current | 2970992 |
Context | intergenic_variant |
Intergenic | 1 |
Allele frequency | 0.493 |
P value | 0.000008 |
Pvalue mlog | 5.09691001300805 |
P value text | |
Or beta | 0.02 |
%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 |