Human SNP ID | rs2556378 |
---|---|
Human chromosome | chr2 |
Human SNP position | 60535367 |
Pig chromosome | chr3 |
Pig SNP position | 85302328 |
PubMed ID | 22012869 |
---|---|
Journal | Am J Med Genet B Neuropsychiatr Genet |
Link | www.ncbi.nlm.nih.gov/pubmed/22012869 |
Study | Genome-wide association study in German patients with attention deficit/hyperactivity disorder. |
Disease/Trait | Attention deficit hyperactivity disorder |
Initial sample | 495 European ancestry child and adolescent cases, 1,300 European ancestry adult controls |
Replication sample | 1,023 European ancestry individuals from 320 families, 2455 European ancestry cases and 896 European ancestry controls from 2,064 trios |
Region | 2p16.1 |
Chromosome id | chr2 |
Chromosome position | 60535367 |
Reported gene | BCL11A |
Mapped gene | BCL11A |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 53335 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs2556378-T |
SNPs | rs2556378 |
Merged | 0 |
SNP id current | 2556378 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | NR |
P value | 0.000007 |
Pvalue mlog | 5.15490195998574 |
P value text | |
Or beta | |
%95 Ci | |
Platform | Illumina [487484] |
CNV | N |
Mapped trait | attention deficit hyperactivity disorder |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0003888 |
Study accession | GCST001287 |