rs1799809
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs1799809(A;A) |
| Make rs1799809(A;G) |
| Make rs1799809(G;G) |
| Reference | GRCh38.p2 38.2/144 |
| Chromosome | 2 |
| Position | 127418299 |
| Gene | PROC |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1799809 |
| dbSNP (classic) | rs1799809 |
| ClinGen | rs1799809 |
| ebi | rs1799809 |
| HLI | rs1799809 |
| Exac | rs1799809 |
| Gnomad | rs1799809 |
| Varsome | rs1799809 |
| LitVar | rs1799809 |
| Map | rs1799809 |
| PheGenI | rs1799809 |
| Biobank | rs1799809 |
| 1000 genomes | rs1799809 |
| hgdp | rs1799809 |
| ensembl | rs1799809 |
| geneview | rs1799809 |
| scholar | rs1799809 |
| rs1799809 | |
| pharmgkb | rs1799809 |
| gwascentral | rs1799809 |
| openSNP | rs1799809 |
| 23andMe | rs1799809 |
| SNPshot | rs1799809 |
| SNPdbe | rs1799809 |
| MSV3d | rs1799809 |
| GWAS Ctlg | rs1799809 |
| Max Magnitude | 0 |
[PMID 24816905
] Single nucleotide variants in the protein C pathway and mortality in dialysis patients
