Human SNP ID | rs4944092 |
---|---|
Human chromosome | chr11 |
Human SNP position | 76198575 |
Pig chromosome | chr9 |
Pig SNP position | 11601412 |
PubMed ID | 20062060 |
---|---|
Journal | Nat Genet |
Link | www.ncbi.nlm.nih.gov/pubmed/20062060 |
Study | Genome-wide association study of PR interval. |
Disease/Trait | PR interval |
Initial sample | 28,517 European ancestry individuals |
Replication sample | NA |
Region | 11q13.5 |
Chromosome id | chr11 |
Chromosome position | 76198575 |
Reported gene | WNT11 |
Mapped gene | WNT11 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 7481 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs4944092-G |
SNPs | rs4944092 |
Merged | 0 |
SNP id current | 4944092 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | 0.32 |
P value | 0.00000003 |
Pvalue mlog | 7.52287874528033 |
P value text | |
Or beta | 1.19 |
%95 Ci | [0.77-1.61] ms decrease |
Platform | Affymetrix, Illumina [~ 2500000] (imputed) |
CNV | N |
Mapped trait | PR interval |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0004462 |
Study accession | GCST000562 |