Human SNP ID | rs4665058 |
---|---|
Human chromosome | chr2 |
Human SNP position | 159333698 |
Pig chromosome | chr15 |
Pig SNP position | 73485426 |
PubMed ID | 21738491 |
---|---|
Journal | PLoS Genet |
Link | www.ncbi.nlm.nih.gov/pubmed/21738491 |
Study | Identification of a sudden cardiac death susceptibility locus at 2q24.2 through genome-wide association in European ancestry individuals. |
Disease/Trait | Sudden cardiac arrest |
Initial sample | 1,283 European ancestry cases, ~20,000 European ancestry controls |
Replication sample | 3,119 European ancestry cases, 11,146 European ancestry controls |
Region | 2q24.2 |
Chromosome id | chr2 |
Chromosome position | 159333698 |
Reported gene | BAZ2B |
Mapped gene | BAZ2B |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 29994 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs4665058-A |
SNPs | rs4665058 |
Merged | 0 |
SNP id current | 4665058 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | 0.014 |
P value | 0.0000000002 |
Pvalue mlog | 9.69897000433601 |
P value text | |
Or beta | 1.92 |
%95 Ci | [1.57-2.34] |
Platform | Affymetrix, Illumina [~ 2500000] (imputed) |
CNV | N |
Mapped trait | sudden cardiac arrest |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0004278 |
Study accession | GCST001132 |