rs4240897
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs4240897(A;A) |
| Make rs4240897(A;G) |
| Make rs4240897(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 11982698 |
| Gene | MFN2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs4240897 |
| dbSNP (classic) | rs4240897 |
| ClinGen | rs4240897 |
| ebi | rs4240897 |
| HLI | rs4240897 |
| Exac | rs4240897 |
| Gnomad | rs4240897 |
| Varsome | rs4240897 |
| LitVar | rs4240897 |
| Map | rs4240897 |
| PheGenI | rs4240897 |
| Biobank | rs4240897 |
| 1000 genomes | rs4240897 |
| hgdp | rs4240897 |
| ensembl | rs4240897 |
| geneview | rs4240897 |
| scholar | rs4240897 |
| rs4240897 | |
| pharmgkb | rs4240897 |
| gwascentral | rs4240897 |
| openSNP | rs4240897 |
| 23andMe | rs4240897 |
| SNPshot | rs4240897 |
| SNPdbe | rs4240897 |
| MSV3d | rs4240897 |
| GWAS Ctlg | rs4240897 |
| GMAF | 0.4477 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
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| ||
[PMID 20940517] HSG/Mfn2 gene polymorphism and essential hypertension: a case-control association study in Chinese
