rs5017717
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs5017717(C;T) |
| Make rs5017717(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 3 |
| Position | 93884869 |
| Gene | PROS1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs5017717 |
| dbSNP (classic) | rs5017717 |
| ClinGen | rs5017717 |
| ebi | rs5017717 |
| HLI | rs5017717 |
| Exac | rs5017717 |
| Gnomad | rs5017717 |
| Varsome | rs5017717 |
| LitVar | rs5017717 |
| Map | rs5017717 |
| PheGenI | rs5017717 |
| Biobank | rs5017717 |
| 1000 genomes | rs5017717 |
| hgdp | rs5017717 |
| ensembl | rs5017717 |
| geneview | rs5017717 |
| scholar | rs5017717 |
| rs5017717 | |
| pharmgkb | rs5017717 |
| gwascentral | rs5017717 |
| openSNP | rs5017717 |
| 23andMe | rs5017717 |
| SNPshot | rs5017717 |
| SNPdbe | rs5017717 |
| MSV3d | rs5017717 |
| GWAS Ctlg | rs5017717 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| ClinVar | |
|---|---|
| Risk | rs5017717(T;T) |
| Alt | rs5017717(T;T) |
| Reference | Rs5017717(C;C) |
| Significance | Untested |
| Disease | |
| Variation | info |
| Gene | PROS1 |
| CLNDBN | OMIM |
| Reversed | 1 |
| HGVS | NC_000003.11:g.93603713G>A |
| CLNSRC | |
| CLNACC | |
