Human SNP ID | rs1533106 |
---|---|
Human chromosome | chr5 |
Human SNP position | 126752020 |
Pig chromosome | chr2 |
Pig SNP position | 135083811 |
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 (total eye scanning length) |
Initial sample | 128 Han Chinese ancestry cases |
Replication sample | NA |
Region | 5q23.2 |
Chromosome id | chr5 |
Chromosome position | 126752020 |
Reported gene | NR |
Mapped gene | LOC102723557 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 102723557 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs1533106-? |
SNPs | rs1533106 |
Merged | |
SNP id current | 1533106 |
Context | non_coding_transcript_exon_variant |
Intergenic | 0 |
Allele frequency | |
P value | 0.000003 |
Pvalue mlog | 5.52287874528033 |
P value text | |
Or beta | 83.03 |
%95 Ci | [47.2-118.86] 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 | GCST003066 |