SNP Detail For rs17346536
1.Mapping Information
Human SNP ID rs17346536
Human chromosome chr1
Human SNP position 173331701
Pig chromosome chr9
Pig SNP position 127354848
2.Annotation Information
PubMed ID25881214
JournalHeart Surg Forum
Linkwww.ncbi.nlm.nih.gov/pubmed/25881214
StudyGenetic variants associated with vein graft stenosis after coronary artery bypass grafting.
Disease/TraitVein graft stenosis in coronary artery bypass grafting
Initial sample361 European ancestry cases, 160 European ancestry controls
Replication sampleNA
Region1q25.1
Chromosome idchr1
Chromosome position173331701
Reported geneTNFSF4
Mapped geneLOC100506023
Upstream gene id
Downstream gene id
SNP gene ids100506023
Upstream gene distance
Downstream gene distance
SNP risk allelers17346536-G
SNPsrs17346536
Merged0
SNP id current17346536
Contextregulatory_region_variant
Intergenic0
Allele frequency0.42
P value0.000009
Pvalue mlog5.04575749056067
P value text
Or beta
%95 Ci
PlatformIllumina [905781]
CNVN
Mapped traitcoronary artery bypass, vein graft stenosis
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0003776, http://www.ebi.ac.uk/efo/EFO_0007051
Study accessionGCST002793