Detailed information
| LncRNA Name | ANRIL |
| Variant Type | SNP |
| Variant ID | rs1333049 |
| Species | human |
| Circulating | ✓ |
| Survival | ✕ |
| CeRNA | ✕ |
| Methylation | ✕ |
| Enhancer | ✕ |
| Drug | ✕ |
| Disease/Trait | myocardial infarction |
| LncRNA Target Gene | NA |
| Tissue | serum |
| Experiment | genotyping |
| Function Description | A strong association of the ANRIL SNP (rs1333049) with MI as well as familial hypercholesterolemia patients in a northern Pakistani population and could be used as a useful genetic marker for the screening of MI in the general Pakistani population. The risk allele C was at a higher frequency in the MI patients as compared to the controls. |
| Pubmed ID | 23266621 |
| Year | 2013 |
| Title | Association of ANRIL polymorphism (rs1333049:C>G) with myocardial infarction and its pharmacogenomic role in hypercholesterolemia |
| External Links | |
|---|---|
| Links For ANRIL | GeneCards HGNC NONCODE LncRNAWiki lncrnadb |
| Links For myocardial infarction | OMIM Cosmic |
| Links For rs1333049 | dbSNP ClinVar OMIM |