Human SNP ID | rs17600642 |
---|---|
Human chromosome | chr10 |
Human SNP position | 70703238 |
Pig chromosome | chr14 |
Pig SNP position | 79440707 |
PubMed ID | 21254220 |
---|---|
Journal | Genet Epidemiol |
Link | www.ncbi.nlm.nih.gov/pubmed/21254220 |
Study | Propensity score-based nonparametric test revealing genetic variants underlying bipolar disorder. |
Disease/Trait | Bipolar disorder |
Initial sample | 1,868 European ancestry cases, 2,938 European ancestry controls |
Replication sample | NA |
Region | 10q22.1 |
Chromosome id | chr10 |
Chromosome position | 70703238 |
Reported gene | NR |
Mapped gene | ADAMTS14 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 140766 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs17600642-? |
SNPs | rs17600642 |
Merged | 0 |
SNP id current | 17600642 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | NR |
P value | 0.000005 |
Pvalue mlog | 5.30102999566398 |
P value text | (addtive) |
Or beta | |
%95 Ci | |
Platform | Affymetrix [NR] |
CNV | N |
Mapped trait | bipolar disorder |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0000289 |
Study accession | GCST000961 |