Human SNP ID | rs4851266 |
---|---|
Human chromosome | chr2 |
Human SNP position | 100202017 |
Pig chromosome | chr3 |
Pig SNP position | 56674969 |
PubMed ID | 23722424 |
---|---|
Journal | Science |
Link | www.ncbi.nlm.nih.gov/pubmed/23722424 |
Study | GWAS of 126,559 individuals identifies genetic variants associated with educational attainment. |
Disease/Trait | Educational attainment |
Initial sample | up to 101,069 European ancestry individuals |
Replication sample | 25,490 European ancestry individuals |
Region | 2q11.2 |
Chromosome id | chr2 |
Chromosome position | 100202017 |
Reported gene | LOC150577 |
Mapped gene | AFF3 - LINC01104 |
Upstream gene id | 3899 |
Downstream gene id | 150577 |
SNP gene ids | |
Upstream gene distance | 59434 |
Downstream gene distance | 6237 |
SNP risk allele | rs4851266-T |
SNPs | rs4851266 |
Merged | 0 |
SNP id current | 4851266 |
Context | intergenic_variant |
Intergenic | 1 |
Allele frequency | 0.396 |
P value | 0.00000000005 |
Pvalue mlog | 10.3010299956639 |
P value text | (College) |
Or beta | 1.05 |
%95 Ci | [NR] |
Platform | Affymetrix, Illumina, Perlegen [up to 2309290] (imputed) |
CNV | N |
Mapped trait | self reported educational attainment |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0004784 |
Study accession | GCST002045 |