rs3813800
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in complete genomics |
| Make rs3813800(C;C) |
| Make rs3813800(C;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 27370983 |
| Gene | FCN3 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs3813800 |
| dbSNP (classic) | rs3813800 |
| ClinGen | rs3813800 |
| ebi | rs3813800 |
| HLI | rs3813800 |
| Exac | rs3813800 |
| Gnomad | rs3813800 |
| Varsome | rs3813800 |
| LitVar | rs3813800 |
| Map | rs3813800 |
| PheGenI | rs3813800 |
| Biobank | rs3813800 |
| 1000 genomes | rs3813800 |
| hgdp | rs3813800 |
| ensembl | rs3813800 |
| geneview | rs3813800 |
| scholar | rs3813800 |
| rs3813800 | |
| pharmgkb | rs3813800 |
| gwascentral | rs3813800 |
| openSNP | rs3813800 |
| 23andMe | rs3813800 |
| SNPshot | rs3813800 |
| SNPdbe | rs3813800 |
| MSV3d | rs3813800 |
| GWAS Ctlg | rs3813800 |
| GMAF | 0.05601 |
| Max Magnitude | 0 |
| ? | (C;C) (C;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 22471352] A Common Genetic Variant of FCN3/CD164L2 Is Associated with Essential Hypertension in a Chinese Population
