Human SNP ID | rs7120489 |
---|---|
Human chromosome | chr11 |
Human SNP position | 12447850 |
Pig chromosome | chr2 |
Pig SNP position | 50360170 |
PubMed ID | 20400778 |
---|---|
Journal | Circ Cardiovasc Genet |
Link | www.ncbi.nlm.nih.gov/pubmed/20400778 |
Study | Genomic 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/Trait | Mortality in heart failure |
Initial sample | 1,645 European ancestry cases, 881 European ancestry controls, 281 African ancestry cases, 185 African ancestry controls |
Replication sample | NA |
Region | 11p15.3 |
Chromosome id | chr11 |
Chromosome position | 12447850 |
Reported gene | PARVA |
Mapped gene | PARVA |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 55742 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs7120489-A |
SNPs | rs7120489 |
Merged | 0 |
SNP id current | 7120489 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | 0.069 |
P value | 0.000007 |
Pvalue mlog | 5.15490195998574 |
P value text | (EA) |
Or beta | 1.35 |
%95 Ci | [0.96-1.90] |
Platform | Affymetrix [up to 2366858] (imputed) |
CNV | N |
Mapped trait | heart failure, mortality |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0003144, http://www.ebi.ac.uk/efo/EFO_0004352 |
Study accession | GCST000661 |