Human SNP ID | rs9599293 |
---|---|
Human chromosome | chr13 |
Human SNP position | 34591253 |
Pig chromosome | chr11 |
Pig SNP position | 10754002 |
PubMed ID | 26242244 |
---|---|
Journal | Sci Rep |
Link | www.ncbi.nlm.nih.gov/pubmed/26242244 |
Study | Association of chromosome 5q21.3 polymorphisms with the exploratory eye movement dysfunction in schizophrenia. |
Disease/Trait | Exploratory eye movement dysfunction in schizophrenia (responsive search score) |
Initial sample | 128 Han Chinese ancestry cases |
Replication sample | NA |
Region | 13q13.2 |
Chromosome id | chr13 |
Chromosome position | 34591253 |
Reported gene | NR |
Mapped gene | LINC00457, LOC105370158 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 100874179, 105370158 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs9599293-? |
SNPs | rs9599293 |
Merged | |
SNP id current | 9599293 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | NR |
P value | 0.000002 |
Pvalue mlog | 5.69897000433601 |
P value text | |
Or beta | 3.033 |
%95 Ci | [1.84-4.23] unit decrease |
Platform | Illumina [498648] |
CNV | N |
Mapped trait | exploratory eye movement measurement |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0007700 |
Study accession | GCST003065 |