Human SNP ID | rs609418 |
---|---|
Human chromosome | chr13 |
Human SNP position | 36843290 |
Pig chromosome | chr11 |
Pig SNP position | 12647996 |
PubMed ID | 25948407 |
---|---|
Journal | BMJ Open |
Link | www.ncbi.nlm.nih.gov/pubmed/25948407 |
Study | Genome-wide association study of perioperative myocardial infarction after coronary artery bypass surgery. |
Disease/Trait | Perioperative myocardial infarction in coronary artery bypass surgery |
Initial sample | 112 cases, 1,321 controls |
Replication sample | 113 European ancestry cases, 509 European ancestry controls |
Region | 13q13.3 |
Chromosome id | chr13 |
Chromosome position | 36843290 |
Reported gene | SMAD9, RFXAP |
Mapped gene | SMAD9 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 4093 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs609418-? |
SNPs | rs609418 |
Merged | |
SNP id current | 609418 |
Context | downstream_gene_variant |
Intergenic | 0 |
Allele frequency | NR |
P value | 0.000006 |
Pvalue mlog | 5.22184874961635 |
P value text | |
Or beta | 1.67 |
%95 Ci | [1.34-2.09] |
Platform | Illumina [534390] |
CNV | N |
Mapped trait | coronary artery bypass, myocardial infarction |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0003776, http://www.ebi.ac.uk/efo/EFO_0000612 |
Study accession | GCST002892 |