SNP Detail For rs7120489
1.Mapping Information
Human SNP ID rs7120489
Human chromosome chr11
Human SNP position 12447850
Pig chromosome chr2
Pig SNP position 50360170
2.Annotation Information
PubMed ID20400778
JournalCirc Cardiovasc Genet
Linkwww.ncbi.nlm.nih.gov/pubmed/20400778
StudyGenomic variation associated with mortality among adults of European and African ancestry with heart failure: the cohorts for heart and aging research in genomic epidemiology consortium.
Disease/TraitMortality in heart failure
Initial sample1,645 European ancestry cases, 881 European ancestry controls, 281 African ancestry cases, 185 African ancestry controls
Replication sampleNA
Region11p15.3
Chromosome idchr11
Chromosome position12447850
Reported genePARVA
Mapped genePARVA
Upstream gene id
Downstream gene id
SNP gene ids55742
Upstream gene distance
Downstream gene distance
SNP risk allelers7120489-A
SNPsrs7120489
Merged0
SNP id current7120489
Contextintron_variant
Intergenic0
Allele frequency0.069
P value0.000007
Pvalue mlog5.15490195998574
P value text(EA)
Or beta1.35
%95 Ci[0.96-1.90]
PlatformAffymetrix [up to 2366858] (imputed)
CNVN
Mapped traitheart failure, mortality
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0003144, http://www.ebi.ac.uk/efo/EFO_0004352
Study accessionGCST000661