Human SNP ID | rs272000 |
---|---|
Human chromosome | chr2 |
Human SNP position | 115898219 |
Pig chromosome | chr15 |
Pig SNP position | 25379001 |
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 | Attention deficit hyperactivity disorder |
Initial sample | 930 European ancestry trios |
Replication sample | NA |
Region | 2q14.1 |
Chromosome id | chr2 |
Chromosome position | 115898219 |
Reported gene | intergenic |
Mapped gene | DPP10 - LOC105373576 |
Upstream gene id | 57628 |
Downstream gene id | 105373576 |
SNP gene ids | |
Upstream gene distance | 52467 |
Downstream gene distance | 396358 |
SNP risk allele | rs272000-? |
SNPs | rs272000 |
Merged | 0 |
SNP id current | 272000 |
Context | intergenic_variant |
Intergenic | 1 |
Allele frequency | NR |
P value | 0.000009 |
Pvalue mlog | 5.04575749056067 |
P value text | (count) |
Or beta | |
%95 Ci | |
Platform | Perlegen [429981] |
CNV | N |
Mapped trait | attention deficit hyperactivity disorder |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0003888 |
Study accession | GCST000281 |