Human SNP ID | rs10765792 |
---|---|
Human chromosome | chr11 |
Human SNP position | 96133536 |
Pig chromosome | chr9 |
Pig SNP position | 32189270 |
PubMed ID | 21658281 |
---|---|
Journal | BMC Cardiovasc Disord |
Link | www.ncbi.nlm.nih.gov/pubmed/21658281 |
Study | GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. |
Disease/Trait | Sudden cardiac arrest |
Initial sample | 88 European ancestry cases, 517 European ancestry controls |
Replication sample | NA |
Region | 11q21 |
Chromosome id | chr11 |
Chromosome position | 96133536 |
Reported gene | intergenic |
Mapped gene | MAML2 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 84441 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs10765792-? |
SNPs | rs10765792 |
Merged | 0 |
SNP id current | 10765792 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | 0.11 |
P value | 0.0000000000008 |
Pvalue mlog | 12.096910013008 |
P value text | (Recessive) |
Or beta | 1.54 |
%95 Ci | [1.37-1.72] |
Platform | Affymetrix [319222] |
CNV | N |
Mapped trait | sudden cardiac arrest |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0004278 |
Study accession | GCST001099 |