Human SNP ID | rs10180522 |
---|---|
Human chromosome | chr2 |
Human SNP position | 145314285 |
Pig chromosome | chr15 |
Pig SNP position | 7095040 |
PubMed ID | 23527680 |
---|---|
Journal | Twin Res Hum Genet |
Link | www.ncbi.nlm.nih.gov/pubmed/23527680 |
Study | Genome-wide association study of inattention and hyperactivity-impulsivity measured as quantitative traits. |
Disease/Trait | Attention deficit hyperactivity disorder (inattention symptoms) |
Initial sample | 1,851 individuals |
Replication sample | 155 individuals |
Region | 2q22.3 |
Chromosome id | chr2 |
Chromosome position | 145314285 |
Reported gene | NR |
Mapped gene | LOC105373661 - LOC105373664 |
Upstream gene id | 105373661 |
Downstream gene id | 105373664 |
SNP gene ids | |
Upstream gene distance | 51078 |
Downstream gene distance | 286636 |
SNP risk allele | rs10180522-A |
SNPs | rs10180522 |
Merged | 0 |
SNP id current | 10180522 |
Context | intron_variant |
Intergenic | 1 |
Allele frequency | |
P value | 0.000007 |
Pvalue mlog | 5.15490195998574 |
P value text | |
Or beta | |
%95 Ci | |
Platform | Illumina [2373249] (imputed) |
CNV | N |
Mapped trait | attention deficit hyperactivity disorder |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0003888 |
Study accession | GCST001943 |