Rs119487098
From SNPedia
| Orientation | plus |
| is a | snp |
| is | mentioned by |
| dbSNP | rs119487098 |
| PheGenI | rs119487098 |
| nextbio | rs119487098 |
| hapmap | rs119487098 |
| 1000 genomes | rs119487098 |
| hgdp | rs119487098 |
| ensembl | rs119487098 |
| gopubmed | rs119487098 |
| geneview | rs119487098 |
| scholar | rs119487098 |
| rs119487098 | |
| pharmgkb | rs119487098 |
| gwascentral | rs119487098 |
| openSNP | rs119487098 |
| 23andMe | rs119487098 |
| 23andMe all | rs119487098 |
| SNP Nexus | |
| SNPshot | rs119487098 |
| SNPdbe | rs119487098 |
| MSV3d | rs119487098 |
| Gene | WWOX |
| Chromosome | 16 |
| Orientation | plus |
| Position | 78466465 |
| Reference | GRCh37 37.1/132 |
| Max Magnitude | 0 |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in complete genomics |
| Make rs119487098(C;C) |
| Make rs119487098(C;T) |
| ClinVar | |
|---|---|
| Risk | rs119487098(C;C) |
| Normal | rs119487098(T;T) |
| Significance | 255 |
| Disease | |
| ClinVar | info |
| Gene | WWOX |
| CLNDBN | |
| Reversed | 0 |
| CLNHGVS | NC_000016.9:g.78466465T>C |
| CLNSRC | |
