Human SNP ID | rs8041675 |
---|---|
Human chromosome | chr15 |
Human SNP position | 37050401 |
Pig chromosome | chr1 |
Pig SNP position | 149925853 |
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 | Hyperactive-impulsive symptoms |
Initial sample | 930 European ancestry trios |
Replication sample | NA |
Region | 15q14 |
Chromosome id | chr15 |
Chromosome position | 37050401 |
Reported gene | MEIS2 |
Mapped gene | MEIS2 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 4212 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs8041675-? |
SNPs | rs8041675 |
Merged | 0 |
SNP id current | 8041675 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | NR |
P value | 0.000004 |
Pvalue mlog | 5.39794000867203 |
P value text | (count) |
Or beta | |
%95 Ci | |
Platform | Perlegen [429981] |
CNV | N |
Mapped trait | behavior |
Mapped trait URI | http://purl.obolibrary.org/obo/GO_0007610 |
Study accession | GCST000278 |