Human SNP ID | rs17346536 |
---|---|
Human chromosome | chr1 |
Human SNP position | 173331701 |
Pig chromosome | chr9 |
Pig SNP position | 127354848 |
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 | 1q25.1 |
Chromosome id | chr1 |
Chromosome position | 173331701 |
Reported gene | TNFSF4 |
Mapped gene | LOC100506023 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 100506023 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs17346536-G |
SNPs | rs17346536 |
Merged | 0 |
SNP id current | 17346536 |
Context | regulatory_region_variant |
Intergenic | 0 |
Allele frequency | 0.42 |
P value | 0.000009 |
Pvalue mlog | 5.04575749056067 |
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 |