Human SNP ID | rs2455601 |
---|---|
Human chromosome | chr11 |
Human SNP position | 8877853 |
Pig chromosome | chr9 |
Pig SNP position | 622491 |
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 | 1,505 Ashkenazi Jewish founder cases, 2,553 Ashkenazi Jewish founder controls |
Replication sample | NA |
Region | 11p15.4 |
Chromosome id | chr11 |
Chromosome position | 8877853 |
Reported gene | NR |
Mapped gene | ST5 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 6764 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs2455601-A |
SNPs | rs2455601 |
Merged | |
SNP id current | 2455601 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | NR |
P value | 0.000007 |
Pvalue mlog | 5.15490195998574 |
P value text | |
Or beta | 1.34 |
%95 Ci | [NR] |
Platform | Illumina [up to 9792010] (imputed) |
CNV | N |
Mapped trait | schizophrenia |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0000692 |
Study accession | GCST003050 |