rs4846085
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs4846085(C;C) |
| Make rs4846085(C;T) |
| Make rs4846085(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 11990577 |
| Gene | MFN2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs4846085 |
| dbSNP (classic) | rs4846085 |
| ClinGen | rs4846085 |
| ebi | rs4846085 |
| HLI | rs4846085 |
| Exac | rs4846085 |
| Gnomad | rs4846085 |
| Varsome | rs4846085 |
| LitVar | rs4846085 |
| Map | rs4846085 |
| PheGenI | rs4846085 |
| Biobank | rs4846085 |
| 1000 genomes | rs4846085 |
| hgdp | rs4846085 |
| ensembl | rs4846085 |
| geneview | rs4846085 |
| scholar | rs4846085 |
| rs4846085 | |
| pharmgkb | rs4846085 |
| gwascentral | rs4846085 |
| openSNP | rs4846085 |
| 23andMe | rs4846085 |
| SNPshot | rs4846085 |
| SNPdbe | rs4846085 |
| MSV3d | rs4846085 |
| GWAS Ctlg | rs4846085 |
| GMAF | 0.3659 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 20940517] HSG/Mfn2 gene polymorphism and essential hypertension: a case-control association study in Chinese
