Human SNP ID | rs6057659 |
---|---|
Human chromosome | chr20 |
Human SNP position | 32857341 |
Pig chromosome | chr17 |
Pig SNP position | 41364018 |
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 | 20q11.21 |
Chromosome id | chr20 |
Chromosome position | 32857341 |
Reported gene | NR |
Mapped gene | MAPRE1 - EFCAB8 |
Upstream gene id | 22919 |
Downstream gene id | 388795 |
SNP gene ids | |
Upstream gene distance | 6936 |
Downstream gene distance | 3654 |
SNP risk allele | rs6057659-A |
SNPs | rs6057659 |
Merged | 0 |
SNP id current | 6057659 |
Context | non_coding_transcript_exon_variant |
Intergenic | 1 |
Allele frequency | |
P value | 0.000005 |
Pvalue mlog | 5.30102999566398 |
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 |