Human SNP ID | rs11617058 |
---|---|
Human chromosome | chr13 |
Human SNP position | 84718977 |
Pig chromosome | chr11 |
Pig SNP position | 61012376 |
PubMed ID | 26198764 |
---|---|
Journal | Am J Med Genet B Neuropsychiatr Genet |
Link | www.ncbi.nlm.nih.gov/pubmed/26198764 |
Study | Genome-wide association study of schizophrenia in Ashkenazi Jews. |
Disease/Trait | Schizophrenia |
Initial sample | 592 Ashkenazi Jewish ancestry cases, 505 Ashkenazi Jewish ancestry controls, 36,989 cases, 113,075 controls |
Replication sample | NA |
Region | 13q31.1 |
Chromosome id | chr13 |
Chromosome position | 84718977 |
Reported gene | NR |
Mapped gene | LOC387939 - LOC105370290 |
Upstream gene id | 387939 |
Downstream gene id | 105370290 |
SNP gene ids | |
Upstream gene distance | 107348 |
Downstream gene distance | 153122 |
SNP risk allele | rs11617058-T |
SNPs | rs11617058 |
Merged | |
SNP id current | 11617058 |
Context | intergenic_variant |
Intergenic | 1 |
Allele frequency | NR |
P value | 0.000001 |
Pvalue mlog | 6 |
P value text | |
Or beta | 1.07 |
%95 Ci | [NR] |
Platform | Illumina [7158791] (imputed) |
CNV | N |
Mapped trait | schizophrenia |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0000692 |
Study accession | GCST003048 |