rs12679196
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in complete genomics |
| Make rs12679196(C;T) |
| Make rs12679196(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 8 |
| Position | 139800104 |
| Gene | TRAPPC9 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs12679196 |
| dbSNP (classic) | rs12679196 |
| ClinGen | rs12679196 |
| ebi | rs12679196 |
| HLI | rs12679196 |
| Exac | rs12679196 |
| Gnomad | rs12679196 |
| Varsome | rs12679196 |
| LitVar | rs12679196 |
| Map | rs12679196 |
| PheGenI | rs12679196 |
| Biobank | rs12679196 |
| 1000 genomes | rs12679196 |
| hgdp | rs12679196 |
| ensembl | rs12679196 |
| geneview | rs12679196 |
| scholar | rs12679196 |
| rs12679196 | |
| pharmgkb | rs12679196 |
| gwascentral | rs12679196 |
| openSNP | rs12679196 |
| 23andMe | rs12679196 |
| SNPshot | rs12679196 |
| SNPdbe | rs12679196 |
| MSV3d | rs12679196 |
| GWAS Ctlg | rs12679196 |
| GMAF | 0.1768 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 20198315] Association of genetic variants with hemorrhagic stroke in Japanese individuals
