Human SNP ID | rs10895959 |
---|---|
Human chromosome | chr11 |
Human SNP position | 106459435 |
Pig chromosome | chr9 |
Pig SNP position | 69538115 |
PubMed ID | 18821565 |
---|---|
Journal | Am J Med Genet B Neuropsychiatr Genet |
Link | www.ncbi.nlm.nih.gov/pubmed/18821565 |
Study | Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations. |
Disease/Trait | Inattentive symptoms |
Initial sample | 930 European ancestry trios |
Replication sample | NA |
Region | 11q22.3 |
Chromosome id | chr11 |
Chromosome position | 106459435 |
Reported gene | intergenic |
Mapped gene | LOC105369474 - LOC105369476 |
Upstream gene id | 105369474 |
Downstream gene id | 105369476 |
SNP gene ids | |
Upstream gene distance | 50251 |
Downstream gene distance | 126555 |
SNP risk allele | rs10895959-? |
SNPs | rs10895959 |
Merged | 0 |
SNP id current | 10895959 |
Context | regulatory_region_variant |
Intergenic | 1 |
Allele frequency | NR |
P value | 0.000003 |
Pvalue mlog | 5.52287874528033 |
P value text | (binary) |
Or beta | |
%95 Ci | |
Platform | Perlegen [429981] |
CNV | N |
Mapped trait | behavior |
Mapped trait URI | http://purl.obolibrary.org/obo/GO_0007610 |
Study accession | GCST000279 |