Human SNP ID | rs11191193 |
---|---|
Human chromosome | chr10 |
Human SNP position | 102042651 |
Pig chromosome | chr14 |
Pig SNP position | 122914142 |
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 | 10q24.32 |
Chromosome id | chr10 |
Chromosome position | 102042651 |
Reported gene | intergenic |
Mapped gene | C10orf76 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 79591 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs11191193-A |
SNPs | rs11191193 |
Merged | 0 |
SNP id current | 11191193 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | 0.653 |
P value | 0.0000006 |
Pvalue mlog | 6.22184874961635 |
P value text | |
Or beta | 0.023 |
%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 |