Human SNP ID | rs4810685 |
---|---|
Human chromosome | chr20 |
Human SNP position | 47771969 |
Pig chromosome | chr17 |
Pig SNP position | 55991389 |
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 | 20q13.12 |
Chromosome id | chr20 |
Chromosome position | 47771969 |
Reported gene | SULF2 |
Mapped gene | SULF2 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 55959 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs4810685-C |
SNPs | rs4810685 |
Merged | 0 |
SNP id current | 4810685 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | NR |
P value | 0.000007 |
Pvalue mlog | 5.15490195998574 |
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 |