rs1799904
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs1799904(A;A) |
| Make rs1799904(A;G) |
| Make rs1799904(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 5 |
| Position | 96429259 |
| Gene | LOC101929710, PCSK1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1799904 |
| dbSNP (classic) | rs1799904 |
| ClinGen | rs1799904 |
| ebi | rs1799904 |
| HLI | rs1799904 |
| Exac | rs1799904 |
| Gnomad | rs1799904 |
| Varsome | rs1799904 |
| LitVar | rs1799904 |
| Map | rs1799904 |
| PheGenI | rs1799904 |
| Biobank | rs1799904 |
| 1000 genomes | rs1799904 |
| hgdp | rs1799904 |
| ensembl | rs1799904 |
| geneview | rs1799904 |
| scholar | rs1799904 |
| rs1799904 | |
| pharmgkb | rs1799904 |
| gwascentral | rs1799904 |
| openSNP | rs1799904 |
| 23andMe | rs1799904 |
| SNPshot | rs1799904 |
| SNPdbe | rs1799904 |
| MSV3d | rs1799904 |
| GWAS Ctlg | rs1799904 |
| GMAF | 0.008724 |
| Max Magnitude | 0 |
[PMID 23383060
] Functional Consequences of a Novel Variant of PCSK1
