Human SNP ID | rs17183295 |
---|---|
Human chromosome | chr17 |
Human SNP position | 32751254 |
Pig chromosome | chr12 |
Pig SNP position | 44003349 |
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 | 17q11.2 |
Chromosome id | chr17 |
Chromosome position | 32751254 |
Reported gene | MYO1D |
Mapped gene | MYO1D |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 4642 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs17183295-T |
SNPs | rs17183295 |
Merged | 0 |
SNP id current | 17183295 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | 0.23 |
P value | 0.0000000001 |
Pvalue mlog | 10 |
P value text | |
Or beta | 0.131 |
%95 Ci | [0.092-0.17] unit decrease |
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 |