SNP Detail For rs7198849
1.Mapping Information
Human SNP ID rs7198849
Human chromosome chr16
Human SNP position 11279444
Pig chromosome chr3
Pig SNP position 32651684
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
Region16p13.13
Chromosome idchr16
Chromosome position11279444
Reported genePRM2
Mapped geneLOC105371082
Upstream gene id
Downstream gene id
SNP gene ids105371082
Upstream gene distance
Downstream gene distance
SNP risk allelers7198849-A
SNPsrs7198849
Merged0
SNP id current7198849
Contextintron_variant
Intergenic0
Allele frequency0.27
P value0.000007
Pvalue mlog5.15490195998574
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