Human SNP ID | rs7866070 |
---|---|
Human chromosome | chr9 |
Human SNP position | 129681820 |
Pig chromosome | chr1 |
Pig SNP position | 303736438 |
PubMed ID | 20585627 |
---|---|
Journal | PLoS Genet |
Link | www.ncbi.nlm.nih.gov/pubmed/20585627 |
Study | Web-based, participant-driven studies yield novel genetic associations for common traits. |
Disease/Trait | Common traits (Other) |
Initial sample | 9,126 European ancestry individuals |
Replication sample | NA |
Region | 9q34.11 |
Chromosome id | chr9 |
Chromosome position | 129681820 |
Reported gene | NR |
Mapped gene | PRRX2 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 51450 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs7866070-? |
SNPs | rs7866070 |
Merged | 0 |
SNP id current | 7866070 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | NR |
P value | 0.0000007 |
Pvalue mlog | 6.15490195998574 |
P value text | (astigmatism) |
Or beta | |
%95 Ci | |
Platform | Illumina [535076] |
CNV | N |
Mapped trait | Astigmatism |
Mapped trait URI | http://purl.obolibrary.org/obo/HP_0000483 |
Study accession | GCST000706 |