Human SNP ID | rs2058350 |
---|---|
Human chromosome | chr12 |
Human SNP position | 3804261 |
Pig chromosome | chr5 |
Pig SNP position | 68796012 |
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 | 12p13.32 |
Chromosome id | chr12 |
Chromosome position | 3804261 |
Reported gene | PARP11 |
Mapped gene | CRACR2A - PARP11 |
Upstream gene id | 84766 |
Downstream gene id | 57097 |
SNP gene ids | |
Upstream gene distance | 51061 |
Downstream gene distance | 4600 |
SNP risk allele | rs2058350-? |
SNPs | rs2058350 |
Merged | 0 |
SNP id current | 2058350 |
Context | intron_variant |
Intergenic | 1 |
Allele frequency | NR |
P value | 0.000008 |
Pvalue mlog | 5.09691001300805 |
P value text | (PC1) |
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 |