rs5935
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs5935(C;T) |
| Make rs5935(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 2 |
| Position | 127428451 |
| Gene | LOC105373608, PROC |
| is a | snp |
| is | mentioned by |
| dbSNP | rs5935 |
| dbSNP (classic) | rs5935 |
| ClinGen | rs5935 |
| ebi | rs5935 |
| HLI | rs5935 |
| Exac | rs5935 |
| Gnomad | rs5935 |
| Varsome | rs5935 |
| LitVar | rs5935 |
| Map | rs5935 |
| PheGenI | rs5935 |
| Biobank | rs5935 |
| 1000 genomes | rs5935 |
| hgdp | rs5935 |
| ensembl | rs5935 |
| geneview | rs5935 |
| scholar | rs5935 |
| rs5935 | |
| pharmgkb | rs5935 |
| gwascentral | rs5935 |
| openSNP | rs5935 |
| 23andMe | rs5935 |
| SNPshot | rs5935 |
| SNPdbe | rs5935 |
| MSV3d | rs5935 |
| GWAS Ctlg | rs5935 |
| GMAF | 0.01423 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs5935(T;T) |
| Alt | rs5935(T;T) |
| Reference | Rs5935(C;C) |
| Significance | Other |
| Disease | Thrombophilia |
| Variation | info |
| Gene | PROC |
| CLNDBN | Thrombophilia, hereditary, due to protein C deficiency, autosomal dominant |
| Reversed | 0 |
| HGVS | NC_000002.11:g.128186027C>T |
| CLNSRC | |
| CLNACC | RCV000233040.2, |
[PMID 17048007
] Association of warfarin dose with genes involved in its action and metabolism.
