Human SNP ID | rs6968385 |
---|---|
Human chromosome | chr7 |
Human SNP position | 110407414 |
Pig chromosome | chr18 |
Pig SNP position | 38097678 |
PubMed ID | 18937294 |
---|---|
Journal | Am J Med Genet B Neuropsychiatr Genet |
Link | www.ncbi.nlm.nih.gov/pubmed/18937294 |
Study | Genome-wide association scan of the time to onset of attention deficit hyperactivity disorder. |
Disease/Trait | Attention deficit hyperactivity disorder (time to onset) |
Initial sample | 930 European ancestry trios |
Replication sample | NA |
Region | 7q31.1 |
Chromosome id | chr7 |
Chromosome position | 110407414 |
Reported gene | intergenic |
Mapped gene | RPL3P8 - LOC105375451 |
Upstream gene id | 646620 |
Downstream gene id | 105375451 |
SNP gene ids | |
Upstream gene distance | 407768 |
Downstream gene distance | 25334 |
SNP risk allele | rs6968385-T |
SNPs | rs6968385 |
Merged | 0 |
SNP id current | 6968385 |
Context | intergenic_variant |
Intergenic | 1 |
Allele frequency | NR |
P value | 0.000002 |
Pvalue mlog | 5.69897000433601 |
P value text | (earlier onset) |
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 | GCST000280 |