Human SNP ID | rs2616984 |
---|---|
Human chromosome | chr8 |
Human SNP position | 4625619 |
Pig chromosome | chr15 |
Pig SNP position | 40976724 |
PubMed ID | 20125193 |
---|---|
Journal | Eur J Hum Genet |
Link | www.ncbi.nlm.nih.gov/pubmed/20125193 |
Study | Common genetic variation and performance on standardized cognitive tests. |
Disease/Trait | Cognitive performance |
Initial sample | Up to 813 European ancestry individuals, up to 167 East Asian ancestry individuals, up to 7 Hispanic/Latin American individuals, up to 74 South Asian ancestry individuals |
Replication sample | NA |
Region | 8p23.2 |
Chromosome id | chr8 |
Chromosome position | 4625619 |
Reported gene | intergenic |
Mapped gene | CSMD1 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 64478 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs2616984-? |
SNPs | rs2616984 |
Merged | 0 |
SNP id current | 2616984 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | NR |
P value | 0.000004 |
Pvalue mlog | 5.39794000867203 |
P value text | (Digit Span Backward) |
Or beta | |
%95 Ci | |
Platform | Illumina [up to 563855] |
CNV | N |
Mapped trait | neuropsychological test |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0003926 |
Study accession | GCST000579 |