Human SNP ID | rs12618769 |
---|---|
Human chromosome | chr2 |
Human SNP position | 98623468 |
Pig chromosome | chr3 |
Pig SNP position | 58215574 |
PubMed ID | 21738484 |
---|---|
Journal | PLoS Genet |
Link | www.ncbi.nlm.nih.gov/pubmed/21738484 |
Study | Genome-wide association of bipolar disorder suggests an enrichment of replicable associations in regions near genes. |
Disease/Trait | Bipolar disorder |
Initial sample | 1,190 European and unknown ancestry cases, 401 European and unknown ancestry controls |
Replication sample | 16,179 individuals |
Region | 2q11.2 |
Chromosome id | chr2 |
Chromosome position | 98623468 |
Reported gene | MGAT4A |
Mapped gene | MGAT4A |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 11320 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs12618769-T |
SNPs | rs12618769 |
Merged | 0 |
SNP id current | 12618769 |
Context | 3_prime_UTR_variant |
Intergenic | 0 |
Allele frequency | NR |
P value | 0.000001 |
Pvalue mlog | 6 |
P value text | |
Or beta | 1.25 |
%95 Ci | [NR] |
Platform | Affymetrix [703019] |
CNV | N |
Mapped trait | bipolar disorder |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0000289 |
Study accession | GCST001135 |