Human SNP ID | rs4763555 |
---|---|
Human chromosome | chr12 |
Human SNP position | 10568857 |
Pig chromosome | chr5 |
Pig SNP position | 64193307 |
PubMed ID | 25644384 |
---|---|
Journal | Mol Psychiatry |
Link | www.ncbi.nlm.nih.gov/pubmed/25644384 |
Study | Genetic contributions to variation in general cognitive function: a meta-analysis of genome-wide association studies in the CHARGE consortium (N=53鈥?49). |
Disease/Trait | Cognitive function |
Initial sample | 51,719 European ancestry individuals 1,473 Erasmus Rupchen Family individuals, 327 Korculan individuals, 430 Orcadian individuals |
Replication sample | NA |
Region | 12p13.2 |
Chromosome id | chr12 |
Chromosome position | 10568857 |
Reported gene | intergenic |
Mapped gene | LOC105376675, LOC101060038 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 105376675, 101060038 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs4763555-? |
SNPs | rs4763555 |
Merged | 0 |
SNP id current | 4763555 |
Context | intergenic_variant |
Intergenic | 0 |
Allele frequency | NR |
P value | 0.000009 |
Pvalue mlog | 5.04575749056067 |
P value text | |
Or beta | 0.0283 |
%95 Ci | [0.016-0.041] unit increase |
Platform | Affymetrix, Illumina [2478500] (imputed) |
CNV | N |
Mapped trait | cognition |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0003925 |
Study accession | GCST002774 |