Detailed information
| LncRNA Name | CCAT2 |
| Variant Type | SNP |
| Variant ID | rs6983267 |
| Species | human |
| Circulating | ✓ |
| Survival | ✕ |
| CeRNA | ✕ |
| Methylation | ✕ |
| Enhancer | ✕ |
| Drug | ✕ |
| Disease/Trait | recurrent miscarriage |
| LncRNA Target Gene | NA |
| Tissue | blood |
| Experiment | genotyping and DNA extraction |
| Function Description | Our study indicates that the rs6983267G allele might contribute to a decreased risk of recurrent miscarriage in the South Chinese population |
| Pubmed ID | 30982978 |
| Year | 2019 |
| Title | The lncRNA CCAT2 rs6983267 G allele is associated with decreased susceptibility to recurrent miscarriage |
| External Links | |
|---|---|
| Links For CCAT2 | GeneCards HGNC NONCODE LncRNAWiki lncrnadb |
| Links For recurrent miscarriage | OMIM Cosmic |
| Links For rs6983267 | dbSNP ClinVar OMIM |