Human SNP ID | rs9918807 |
---|---|
Human chromosome | chr8 |
Human SNP position | 129664393 |
Pig chromosome | chr4 |
Pig SNP position | 11019428 |
PubMed ID | 23393555 |
---|---|
Journal | PLoS One |
Link | www.ncbi.nlm.nih.gov/pubmed/23393555 |
Study | Genome-wide association study of retinopathy in individuals without diabetes. |
Disease/Trait | Retinopathy in non-diabetics |
Initial sample | 19,411 European ancestry individuals |
Replication sample | NA |
Region | 8q24.21 |
Chromosome id | chr8 |
Chromosome position | 129664393 |
Reported gene | MLZE |
Mapped gene | CCDC26 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 137196 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs9918807-T |
SNPs | rs9918807 |
Merged | 0 |
SNP id current | 9918807 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | 0.94 |
P value | 0.000005 |
Pvalue mlog | 5.30102999566398 |
P value text | |
Or beta | 0.47 |
%95 Ci | [0.27-0.67] unit decrease |
Platform | Illumina [2675979] (imputed) |
CNV | N |
Mapped trait | retinopathy |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0003839 |
Study accession | GCST001854 |