Human SNP ID | rs391760 |
---|---|
Human chromosome | chr5 |
Human SNP position | 144031781 |
Pig chromosome | chr2 |
Pig SNP position | 151919596 |
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 | 5q31.3 |
Chromosome id | chr5 |
Chromosome position | 144031781 |
Reported gene | NR |
Mapped gene | HMHB1 - YIPF5 |
Upstream gene id | 57824 |
Downstream gene id | 81555 |
SNP gene ids | |
Upstream gene distance | 211062 |
Downstream gene distance | 126378 |
SNP risk allele | rs391760-? |
SNPs | rs391760 |
Merged | 0 |
SNP id current | 391760 |
Context | intergenic_variant |
Intergenic | 1 |
Allele frequency | NR |
P value | 0.000002 |
Pvalue mlog | 5.69897000433601 |
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 |