Human SNP ID | rs4681767 |
---|---|
Human chromosome | chr3 |
Human SNP position | 56725664 |
Pig chromosome | chr13 |
Pig SNP position | 42428260 |
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 | 3p14.3 |
Chromosome id | chr3 |
Chromosome position | 56725664 |
Reported gene | ARHGEF3 |
Mapped gene | FAM208A - ARHGEF3 |
Upstream gene id | 23272 |
Downstream gene id | 50650 |
SNP gene ids | |
Upstream gene distance | 42422 |
Downstream gene distance | 1754 |
SNP risk allele | rs4681767-T |
SNPs | rs4681767 |
Merged | |
SNP id current | 4681767 |
Context | downstream_gene_variant |
Intergenic | 1 |
Allele frequency | 0.429 |
P value | 0.000008 |
Pvalue mlog | 5.09691001300805 |
P value text | (IIV) |
Or beta | 0.18 |
%95 Ci | [0.1-0.26] 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 |