Human SNP ID | rs7198849 |
---|---|
Human chromosome | chr16 |
Human SNP position | 11279444 |
Pig chromosome | chr3 |
Pig SNP position | 32651684 |
PubMed ID | 25881214 |
---|---|
Journal | Heart Surg Forum |
Link | www.ncbi.nlm.nih.gov/pubmed/25881214 |
Study | Genetic variants associated with vein graft stenosis after coronary artery bypass grafting. |
Disease/Trait | Vein graft stenosis in coronary artery bypass grafting |
Initial sample | 361 European ancestry cases, 160 European ancestry controls |
Replication sample | NA |
Region | 16p13.13 |
Chromosome id | chr16 |
Chromosome position | 11279444 |
Reported gene | PRM2 |
Mapped gene | LOC105371082 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 105371082 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs7198849-A |
SNPs | rs7198849 |
Merged | 0 |
SNP id current | 7198849 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | 0.27 |
P value | 0.000007 |
Pvalue mlog | 5.15490195998574 |
P value text | |
Or beta | |
%95 Ci | |
Platform | Illumina [905781] |
CNV | N |
Mapped trait | coronary artery bypass, vein graft stenosis |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0003776, http://www.ebi.ac.uk/efo/EFO_0007051 |
Study accession | GCST002793 |