Detailed information
| LncRNA Name | H19 |
| Variant Type | SNP |
| Variant ID | rs2067051 |
| Species | human |
| Circulating | ✓ |
| Survival | ✕ |
| CeRNA | ✕ |
| Methylation | ✕ |
| Enhancer | ✕ |
| Drug | ✕ |
| Disease/Trait | coronary artery disease |
| LncRNA Target Gene | NA |
| Tissue | blood |
| Experiment | genotyping |
| Function Description | The A variant of H19 SNP rs2067051 was associated with a decreased risk of CAD. |
| Pubmed ID | 25772106 |
| Year | 2015 |
| Title | Association of polymorphisms in long non-coding RNA H19 with coronary artery disease risk in a Chinese population |
| External Links | |
|---|---|
| Links For H19 | GeneCards HGNC NONCODE LncRNAWiki lncrnadb |
| Links For coronary artery disease | OMIM Cosmic |
| Links For rs2067051 | dbSNP ClinVar OMIM |