rs16936752
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in complete genomics |
| Make rs16936752(G;G) |
| Make rs16936752(G;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 9 |
| Position | 93301408 |
| Gene | WNK2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs16936752 |
| dbSNP (classic) | rs16936752 |
| ClinGen | rs16936752 |
| ebi | rs16936752 |
| HLI | rs16936752 |
| Exac | rs16936752 |
| Gnomad | rs16936752 |
| Varsome | rs16936752 |
| LitVar | rs16936752 |
| Map | rs16936752 |
| PheGenI | rs16936752 |
| Biobank | rs16936752 |
| 1000 genomes | rs16936752 |
| hgdp | rs16936752 |
| ensembl | rs16936752 |
| geneview | rs16936752 |
| scholar | rs16936752 |
| rs16936752 | |
| pharmgkb | rs16936752 |
| gwascentral | rs16936752 |
| openSNP | rs16936752 |
| 23andMe | rs16936752 |
| SNPshot | rs16936752 |
| SNPdbe | rs16936752 |
| MSV3d | rs16936752 |
| GWAS Ctlg | rs16936752 |
| GMAF | 0.08907 |
| Max Magnitude | 0 |
| ? | (G;G) (G;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 20198315] Association of genetic variants with hemorrhagic stroke in Japanese individuals
