SNP Detail For rs13225783
1.Mapping Information
Human SNP ID rs13225783
Human chromosome chr7
Human SNP position 27290437
Pig chromosome chr18
Pig SNP position 49928608
2.Annotation Information
PubMed ID20445134
JournalCirc Cardiovasc Genet
Linkwww.ncbi.nlm.nih.gov/pubmed/20445134
StudyAssociation of genome-wide variation with the risk of incident heart failure in adults of European and African ancestry: a prospective meta-analysis from the cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium.
Disease/TraitHeart failure
Initial sample20,926 European ancestry individuals, 2,895 African ancestry individuals
Replication sampleNA
Region7p15.2
Chromosome idchr7
Chromosome position27290437
Reported geneEVX1
Mapped geneRPL35P4 - LOC105375206
Upstream gene id100271006
Downstream gene id105375206
SNP gene ids
Upstream gene distance20684
Downstream gene distance89496
SNP risk allelers13225783-?
SNPsrs13225783
Merged0
SNP id current13225783
Contextintergenic_variant
Intergenic1
Allele frequency0.05
P value0.000007
Pvalue mlog5.15490195998574
P value text(EA)
Or beta1.38
%95 Ci[0.96-1.99]
PlatformAffymetrix, Illumina [2478304] (imputed)
CNVN
Mapped traitheart failure
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0003144
Study accessionGCST000675