Human SNP ID | rs2867695 |
---|---|
Human chromosome | chr4 |
Human SNP position | 80152066 |
Pig chromosome | chr8 |
Pig SNP position | 146829005 |
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 | 4q21.21 |
Chromosome id | chr4 |
Chromosome position | 80152066 |
Reported gene | PRDM8 |
Mapped gene | LOC643513 - RPSAP39 |
Upstream gene id | 643513 |
Downstream gene id | 100131161 |
SNP gene ids | |
Upstream gene distance | 70698 |
Downstream gene distance | 8987 |
SNP risk allele | rs2867695-? |
SNPs | rs2867695 |
Merged | |
SNP id current | 2867695 |
Context | intergenic_variant |
Intergenic | 1 |
Allele frequency | NR |
P value | 0.000004 |
Pvalue mlog | 5.39794000867203 |
P value text | |
Or beta | 1.412 |
%95 Ci | [0.84-1.99] 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 |