Human SNP ID | rs1918172 |
---|---|
Human chromosome | chr2 |
Human SNP position | 156031988 |
Pig chromosome | chr15 |
Pig SNP position | 70324332 |
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 | 2q24.1 |
Chromosome id | chr2 |
Chromosome position | 156031988 |
Reported gene | intergenic |
Mapped gene | LOC101929378 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 101929378 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs1918172-? |
SNPs | rs1918172 |
Merged | 0 |
SNP id current | 1918172 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | NR |
P value | 0.000005 |
Pvalue mlog | 5.30102999566398 |
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 |