Human SNP ID | rs663734 |
---|---|
Human chromosome | chr11 |
Human SNP position | 125114959 |
Pig chromosome | chr9 |
Pig SNP position | 57820067 |
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 (cognitive search score) |
Initial sample | 128 Han Chinese ancestry cases |
Replication sample | NA |
Region | 11q24.2 |
Chromosome id | chr11 |
Chromosome position | 125114959 |
Reported gene | LOC399965 |
Mapped gene | KRT18P59 - PKNOX2-AS1 |
Upstream gene id | 399965 |
Downstream gene id | 103695364 |
SNP gene ids | |
Upstream gene distance | 40 |
Downstream gene distance | 43502 |
SNP risk allele | rs663734-? |
SNPs | rs663734 |
Merged | |
SNP id current | 663734 |
Context | intron_variant |
Intergenic | 1 |
Allele frequency | NR |
P value | 0.000005 |
Pvalue mlog | 5.30102999566398 |
P value text | |
Or beta | 2.254 |
%95 Ci | [1.32-3.18] 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 | GCST003064 |