Human SNP ID | rs10453441 |
---|---|
Human chromosome | chr22 |
Human SNP position | 45967859 |
Pig chromosome | chr5 |
Pig SNP position | 703105 |
PubMed ID | 25823570 |
---|---|
Journal | Nat Commun |
Link | www.ncbi.nlm.nih.gov/pubmed/25823570 |
Study | Identification of myopia-associated WNT7B polymorphisms provides insights into the mechanism underlying the development of myopia. |
Disease/Trait | Corneal curvature |
Initial sample | Up to 3,248 Japanese ancestry individuals |
Replication sample | 6,234 East Asian ancestry individuals, 2,007 European ancestry individuals |
Region | 22q13.31 |
Chromosome id | chr22 |
Chromosome position | 45967859 |
Reported gene | WNT7B |
Mapped gene | WNT7B |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 7477 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs10453441-A |
SNPs | rs10453441 |
Merged | 0 |
SNP id current | 10453441 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | 0.33 |
P value | 3E-40 |
Pvalue mlog | 39.5228787452803 |
P value text | |
Or beta | 0.051 |
%95 Ci | [0.043-0.059] unit increase |
Platform | Illumina [1773334] (imputed) |
CNV | N |
Mapped trait | corneal topography |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0004345 |
Study accession | GCST002834 |