Human SNP ID | rs10153620 |
---|---|
Human chromosome | chr2 |
Human SNP position | 205195913 |
Pig chromosome | chr15 |
Pig SNP position | 120026587 |
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 (combined symptoms) |
Initial sample | 1,851 individuals |
Replication sample | 155 individuals |
Region | 2q33.3 |
Chromosome id | chr2 |
Chromosome position | 205195913 |
Reported gene | NR |
Mapped gene | PARD3B |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 117583 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs10153620-C |
SNPs | rs10153620 |
Merged | 0 |
SNP id current | 10153620 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | |
P value | 0.000006 |
Pvalue mlog | 5.22184874961635 |
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 | GCST001931 |