rs115232898
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in clinvar |
| Make rs115232898(C;C) |
| Make rs115232898(C;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 1 |
| Position | 97699474 |
| Gene | DPYD |
| is a | snp |
| is | mentioned by |
| dbSNP | rs115232898 |
| dbSNP (classic) | rs115232898 |
| ClinGen | rs115232898 |
| ebi | rs115232898 |
| HLI | rs115232898 |
| Exac | rs115232898 |
| Gnomad | rs115232898 |
| Varsome | rs115232898 |
| LitVar | rs115232898 |
| Map | rs115232898 |
| PheGenI | rs115232898 |
| Biobank | rs115232898 |
| 1000 genomes | rs115232898 |
| hgdp | rs115232898 |
| ensembl | rs115232898 |
| geneview | rs115232898 |
| scholar | rs115232898 |
| rs115232898 | |
| pharmgkb | rs115232898 |
| gwascentral | rs115232898 |
| openSNP | rs115232898 |
| 23andMe | rs115232898 |
| SNPshot | rs115232898 |
| SNPdbe | rs115232898 |
| MSV3d | rs115232898 |
| GWAS Ctlg | rs115232898 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs115232898(C;C) |
| Alt | rs115232898(C;C) |
| Reference | Rs115232898(T;T) |
| Significance | Untested |
| Disease | not provided |
| Variation | info |
| Gene | DPYD |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000001.10:g.98165030T>C |
| CLNSRC | ClinVar |
| CLNACC | RCV000086496.1, |
