Human SNP ID | rs2699783 |
---|---|
Human chromosome | chr2 |
Human SNP position | 66031567 |
Pig chromosome | chr3 |
Pig SNP position | 79748514 |
PubMed ID | 24322204 |
---|---|
Journal | Mol Psychiatry |
Link | www.ncbi.nlm.nih.gov/pubmed/24322204 |
Study | Genome-wide association study of bipolar disorder accounting for effect of body mass index identifies a new risk allele in TCF7L2. |
Disease/Trait | Bipolar disorder (body mass index interaction) |
Initial sample | 388 European ancestry cases, 1,020 European ancestry controls |
Replication sample | NA |
Region | 2p14 |
Chromosome id | chr2 |
Chromosome position | 66031567 |
Reported gene | MIR4778 |
Mapped gene | LOC105369168 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 105369168 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs2699783-? |
SNPs | rs2699783 |
Merged | 0 |
SNP id current | 2699783 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | NR |
P value | 0.000007 |
Pvalue mlog | 5.15490195998574 |
P value text | |
Or beta | |
%95 Ci | |
Platform | NR [up to 8466825] (imputed) |
CNV | N |
Mapped trait | bipolar disorder, body mass index |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0000289, http://www.ebi.ac.uk/efo/EFO_0004340 |
Study accession | GCST002306 |