Human SNP ID | rs7837791 |
---|---|
Human chromosome | chr8 |
Human SNP position | 59266527 |
Pig chromosome | chr4 |
Pig SNP position | 80455558 |
PubMed ID | 23396134 |
---|---|
Journal | Nat Genet |
Link | www.ncbi.nlm.nih.gov/pubmed/23396134 |
Study | Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia. |
Disease/Trait | Refractive error |
Initial sample | 37,382 European ancestry individuals, 3,995 Chinese ancestry individuals, 2,273 Malay ancestry individuals, 2,108 Indian ancestry individuals |
Replication sample | NA |
Region | 8q12.1 |
Chromosome id | chr8 |
Chromosome position | 59266527 |
Reported gene | CHD7, TOX |
Mapped gene | LOC100505501 - NUDT15P1 |
Upstream gene id | 100505501 |
Downstream gene id | 574532 |
SNP gene ids | |
Upstream gene distance | 145180 |
Downstream gene distance | 290172 |
SNP risk allele | rs7837791-T |
SNPs | rs7837791 |
Merged | 0 |
SNP id current | 7837791 |
Context | intergenic_variant |
Intergenic | 1 |
Allele frequency | 0.49 |
P value | 0.000000000004 |
Pvalue mlog | 11.397940008672 |
P value text | |
Or beta | 0.106 |
%95 Ci | [0.077-0.135] unit increase |
Platform | Affymetrix, Illumina [2500000] (imputed) |
CNV | N |
Mapped trait | Abnormality of refraction |
Mapped trait URI | http://purl.obolibrary.org/obo/HP_0000539 |
Study accession | GCST001858 |