Human SNP ID | rs2111902 |
---|---|
Human chromosome | chr12 |
Human SNP position | 108884971 |
Pig chromosome | chr14 |
Pig SNP position | 44487544 |
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 (mean eye scanning length) |
Initial sample | 128 Han Chinese ancestry cases |
Replication sample | NA |
Region | 12q24.11 |
Chromosome id | chr12 |
Chromosome position | 108884971 |
Reported gene | NR |
Mapped gene | DAO |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 1610 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs2111902-? |
SNPs | rs2111902 |
Merged | |
SNP id current | 2111902 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | |
P value | 0.0000002 |
Pvalue mlog | 6.69897000433601 |
P value text | |
Or beta | 4.428 |
%95 Ci | [2.84-6.02] unit increase |
Platform | Illumina [498648] |
CNV | N |
Mapped trait | exploratory eye movement measurement |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0007700 |
Study accession | GCST003067 |