Human SNP ID | rs282544 |
---|---|
Human chromosome | chr5 |
Human SNP position | 50730631 |
Pig chromosome | chr16 |
Pig SNP position | 31949832 |
PubMed ID | 22685421 |
---|---|
Journal | PLoS Genet |
Link | www.ncbi.nlm.nih.gov/pubmed/22685421 |
Study | Genetic variants on chromosome 1q41 influence ocular axial length and high myopia. |
Disease/Trait | Myopia (pathological) |
Initial sample | 2,789 Chinese ancestry individuals, 2,155 Malay ancestry individuals |
Replication sample | NA |
Region | 5q11.1 |
Chromosome id | chr5 |
Chromosome position | 50730631 |
Reported gene | PARP8 |
Mapped gene | PARP8 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 79668 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs282544-C |
SNPs | rs282544 |
Merged | 0 |
SNP id current | 282544 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | 0.35 |
P value | 0.000004 |
Pvalue mlog | 5.39794000867203 |
P value text | |
Or beta | 0.1 |
%95 Ci | [0.061-0.139] mm decrease |
Platform | Illumina [456634] |
CNV | N |
Mapped trait | pathological myopia |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0004207 |
Study accession | GCST001561 |