rs897984
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs897984(A;A) |
| Make rs897984(A;G) |
| Make rs897984(G;G) |
| Reference | GRCh38.p2 38.2/146 |
| Chromosome | 16 |
| Position | 30875322 |
| Gene | BCL7C, MIR762HG, MIR4519 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs897984 |
| dbSNP (classic) | rs897984 |
| ClinGen | rs897984 |
| ebi | rs897984 |
| HLI | rs897984 |
| Exac | rs897984 |
| Gnomad | rs897984 |
| Varsome | rs897984 |
| LitVar | rs897984 |
| Map | rs897984 |
| PheGenI | rs897984 |
| Biobank | rs897984 |
| 1000 genomes | rs897984 |
| hgdp | rs897984 |
| ensembl | rs897984 |
| geneview | rs897984 |
| scholar | rs897984 |
| rs897984 | |
| pharmgkb | rs897984 |
| gwascentral | rs897984 |
| openSNP | rs897984 |
| 23andMe | rs897984 |
| SNPshot | rs897984 |
| SNPdbe | rs897984 |
| MSV3d | rs897984 |
| GWAS Ctlg | rs897984 |
| Max Magnitude | 0 |
[PMID 26670097] Genetic Variants in MicroRNAs and their Binding Sites are Associated with the Risk of Parkinson Disease
