Human SNP ID | rs4450798 |
---|---|
Human chromosome | chr3 |
Human SNP position | 13695501 |
Pig chromosome | chr13 |
Pig SNP position | 78203970 |
PubMed ID | 23092984 |
---|---|
Journal | Transl Psychiatry |
Link | www.ncbi.nlm.nih.gov/pubmed/23092984 |
Study | Genome-wide association of mood-incongruent psychotic bipolar disorder. |
Disease/Trait | Bipolar disorder with mood-incongruent psychosis |
Initial sample | 2,196 European and other ancestry cases, 8,148 European and other ancestry controls |
Replication sample | NA |
Region | 3p25.1 |
Chromosome id | chr3 |
Chromosome position | 13695501 |
Reported gene | FBLN2 |
Mapped gene | LINC00620 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 285375 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs4450798-T |
SNPs | rs4450798 |
Merged | 0 |
SNP id current | 4450798 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | NR |
P value | 0.000002 |
Pvalue mlog | 5.69897000433601 |
P value text | |
Or beta | 1.26 |
%95 Ci | [NR] |
Platform | Affymetrix, Illumina [~ 2500000] (imputed) |
CNV | N |
Mapped trait | bipolar disorder |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0000289 |
Study accession | GCST001715 |