Human SNP ID | rs1422110 |
---|---|
Human chromosome | chr5 |
Human SNP position | 86170322 |
Pig chromosome | chr2 |
Pig SNP position | 96449715 |
PubMed ID | 26174813 |
---|---|
Journal | Am J Med Genet B Neuropsychiatr Genet |
Link | www.ncbi.nlm.nih.gov/pubmed/26174813 |
Study | New suggestive genetic loci and biological pathways for attention function in adult attention-deficit/hyperactivity disorder. |
Disease/Trait | Attention function in attention deficit hyperactive disorder |
Initial sample | 479 European ancestry adult cases |
Replication sample | NA |
Region | 5q14.3 |
Chromosome id | chr5 |
Chromosome position | 86170322 |
Reported gene | NBPF22P |
Mapped gene | LOC105379063 - NBPF22P |
Upstream gene id | 105379063 |
Downstream gene id | 285622 |
SNP gene ids | |
Upstream gene distance | 139219 |
Downstream gene distance | 112122 |
SNP risk allele | rs1422110-G |
SNPs | rs1422110 |
Merged | |
SNP id current | 1422110 |
Context | intergenic_variant |
Intergenic | 1 |
Allele frequency | 0.46 |
P value | 0.000008 |
Pvalue mlog | 5.09691001300805 |
P value text | (IIV) |
Or beta | 0.19 |
%95 Ci | [0.11-0.27] unit decrease |
Platform | Illumina [799713] |
CNV | N |
Mapped trait | attention deficit hyperactivity disorder, attention function measurement |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0003888, http://www.ebi.ac.uk/efo/EFO_0007636 |
Study accession | GCST003025 |