Human SNP ID | rs1472750 |
---|---|
Human chromosome | chr10 |
Human SNP position | 113475355 |
Pig chromosome | chr14 |
Pig SNP position | 135080384 |
PubMed ID | 23049088 |
---|---|
Journal | Invest Ophthalmol Vis Sci |
Link | www.ncbi.nlm.nih.gov/pubmed/23049088 |
Study | A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population. |
Disease/Trait | Myopia (pathological) |
Initial sample | 187 European ancestry cases, 1064 European ancestry controls |
Replication sample | |
Region | 10q25.3 |
Chromosome id | chr10 |
Chromosome position | 113475355 |
Reported gene | intergenic |
Mapped gene | LOC105378490 - LOC101927654 |
Upstream gene id | 105378490 |
Downstream gene id | 101927654 |
SNP gene ids | |
Upstream gene distance | 154384 |
Downstream gene distance | 6685 |
SNP risk allele | rs1472750-? |
SNPs | rs1472750 |
Merged | 0 |
SNP id current | 1472750 |
Context | regulatory_region_variant |
Intergenic | 1 |
Allele frequency | 0.075 |
P value | 0.000000005 |
Pvalue mlog | 8.30102999566398 |
P value text | |
Or beta | |
%95 Ci | [NR] |
Platform | Affymetrix, Illumina [152234] |
CNV | N |
Mapped trait | pathological myopia |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0004207 |
Study accession | GCST001712 |