Human SNP ID | rs6060821 |
---|---|
Human chromosome | chr20 |
Human SNP position | 31706231 |
Pig chromosome | chr17 |
Pig SNP position | 40237981 |
PubMed ID | 26184070 |
---|---|
Journal | Am J Med Genet B Neuropsychiatr Genet |
Link | www.ncbi.nlm.nih.gov/pubmed/26184070 |
Study | Gene-set and multivariate genome-wide association analysis of oppositional defiant behavior subtypes in attention-deficit/hyperactivity disorder. |
Disease/Trait | Oppositional defiant disorder in attention-deficit hyperactivity disorder |
Initial sample | 750 European ancestry individuals |
Replication sample | NA |
Region | 20q11.21 |
Chromosome id | chr20 |
Chromosome position | 31706231 |
Reported gene | BCL2L1, COX4I2, TPX2, MYLK2, TTLL9, FOXS1 |
Mapped gene | BCL2L1, LOC105372589 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 598, 105372589 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs6060821-? |
SNPs | rs6060821 |
Merged | |
SNP id current | 6060821 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | NR |
P value | 0.000004 |
Pvalue mlog | 5.39794000867203 |
P value text | |
Or beta | |
%95 Ci | |
Platform | Perlegen [1871025] (imputed) |
CNV | N |
Mapped trait | attention deficit hyperactivity disorder, oppositional defiant disorder measurement |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0003888, http://www.ebi.ac.uk/efo/EFO_0007679 |
Study accession | GCST003030 |