Home Details
| Official Symbol of Gene | MIR196A2 |
| Species | Homo sapiens |
| Entrez Gene ID | 406973 |
| Official Full Name | microRNA 196a-2 |
| Also known as | MIRN196-2; MIRN196A2; mir-196a-2 |
| Gene Type | ncRNA |
| dbXrefs | Ensembl:ENSG00000207924 MIM:609687; miRBase:MI0000279; AllianceGenome:HGNC:31568 |
| Map Location | 12q13.13 |
| Variation Type | SNP |
| refSNP ID | rs11614913 |
| Detected Sample | Blood |
| Sample Detail | N/A |
| Detected Method | PCR |
| Disease | MS |
| Disease subtype | N/A |
| Population | Isfahan |
| Sample Size | 80 patients and the same number control |
| Pubmed ID | 30518189 |
| Year | 2018 |
| Title | Genetic Variation in Intergenic and Exonic miRNA Sequence and Risk of Multiple Sclerosis in the Isfahan Patients |
| Risk Type | N/A |
| Main Result | negative |
| Result | These results showed that individuals carrying the genotypes of rs3745453 TC had a 2.3-fold increased risk of MS (OR=2.3, p=0.048). There was no significant difference between genotypes and allele frequency of mir155 and mir196a2 in patients and healthy controls. |
| Mechanism/Pathway | N/A |

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