Human SNP ID | rs6758152 |
---|---|
Human chromosome | chr2 |
Human SNP position | 104051280 |
Pig chromosome | chr3 |
Pig SNP position | 52828400 |
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 (hyperactivity-impulsivity symptoms) |
Initial sample | 1,851 individuals |
Replication sample | 155 individuals |
Region | 2q12.1 |
Chromosome id | chr2 |
Chromosome position | 104051280 |
Reported gene | NR |
Mapped gene | LOC105373520 - LOC105373521 |
Upstream gene id | 105373520 |
Downstream gene id | 105373521 |
SNP gene ids | |
Upstream gene distance | 231112 |
Downstream gene distance | 42338 |
SNP risk allele | rs6758152-T |
SNPs | rs6758152 |
Merged | 0 |
SNP id current | 6758152 |
Context | intron_variant |
Intergenic | 1 |
Allele frequency | |
P value | 0.000003 |
Pvalue mlog | 5.52287874528033 |
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 | GCST001944 |