Human SNP ID | rs41297816 |
---|---|
Human chromosome | chr22 |
Human SNP position | 19776455 |
Pig chromosome | chr14 |
Pig SNP position | 54940330 |
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 | 22q11.21 |
Chromosome id | chr22 |
Chromosome position | 19776455 |
Reported gene | TBX1, GNB1L |
Mapped gene | TBX1 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 6899 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs41297816-G |
SNPs | rs41297816 |
Merged | |
SNP id current | 41297816 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | NR |
P value | 0.0000001 |
Pvalue mlog | 7 |
P value text | |
Or beta | 1.3513513 |
%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 |