rs707916
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs707916(C;C) |
| Make rs707916(C;T) |
| Make rs707916(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 31729781 |
| Gene | DDAH2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs707916 |
| dbSNP (classic) | rs707916 |
| ClinGen | rs707916 |
| ebi | rs707916 |
| HLI | rs707916 |
| Exac | rs707916 |
| Gnomad | rs707916 |
| Varsome | rs707916 |
| LitVar | rs707916 |
| Map | rs707916 |
| PheGenI | rs707916 |
| Biobank | rs707916 |
| 1000 genomes | rs707916 |
| hgdp | rs707916 |
| ensembl | rs707916 |
| geneview | rs707916 |
| scholar | rs707916 |
| rs707916 | |
| pharmgkb | rs707916 |
| gwascentral | rs707916 |
| openSNP | rs707916 |
| 23andMe | rs707916 |
| SNPshot | rs707916 |
| SNPdbe | rs707916 |
| MSV3d | rs707916 |
| GWAS Ctlg | rs707916 |
| GMAF | 0.4738 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 19250061] Common genetic variation in DDAH2 is associated with intracerebral hemorrhage in Chinese population: a multicenter case-control study in China.
