Human SNP ID | rs13225783 |
---|---|
Human chromosome | chr7 |
Human SNP position | 27290437 |
Pig chromosome | chr18 |
Pig SNP position | 49928608 |
PubMed ID | 20445134 |
---|---|
Journal | Circ Cardiovasc Genet |
Link | www.ncbi.nlm.nih.gov/pubmed/20445134 |
Study | Association 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/Trait | Heart failure |
Initial sample | 20,926 European ancestry individuals, 2,895 African ancestry individuals |
Replication sample | NA |
Region | 7p15.2 |
Chromosome id | chr7 |
Chromosome position | 27290437 |
Reported gene | EVX1 |
Mapped gene | RPL35P4 - LOC105375206 |
Upstream gene id | 100271006 |
Downstream gene id | 105375206 |
SNP gene ids | |
Upstream gene distance | 20684 |
Downstream gene distance | 89496 |
SNP risk allele | rs13225783-? |
SNPs | rs13225783 |
Merged | 0 |
SNP id current | 13225783 |
Context | intergenic_variant |
Intergenic | 1 |
Allele frequency | 0.05 |
P value | 0.000007 |
Pvalue mlog | 5.15490195998574 |
P value text | (EA) |
Or beta | 1.38 |
%95 Ci | [0.96-1.99] |
Platform | Affymetrix, Illumina [2478304] (imputed) |
CNV | N |
Mapped trait | heart failure |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0003144 |
Study accession | GCST000675 |