rs992670
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs992670(A;A) |
| Make rs992670(A;G) |
| Make rs992670(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 9 |
| Position | 121019492 |
| Gene | C5 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs992670 |
| dbSNP (classic) | rs992670 |
| ClinGen | rs992670 |
| ebi | rs992670 |
| HLI | rs992670 |
| Exac | rs992670 |
| Gnomad | rs992670 |
| Varsome | rs992670 |
| LitVar | rs992670 |
| Map | rs992670 |
| PheGenI | rs992670 |
| Biobank | rs992670 |
| 1000 genomes | rs992670 |
| hgdp | rs992670 |
| ensembl | rs992670 |
| geneview | rs992670 |
| scholar | rs992670 |
| rs992670 | |
| pharmgkb | rs992670 |
| gwascentral | rs992670 |
| openSNP | rs992670 |
| 23andMe | rs992670 |
| SNPshot | rs992670 |
| SNPdbe | rs992670 |
| MSV3d | rs992670 |
| GWAS Ctlg | rs992670 |
| GMAF | 0.4068 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 19909405] Single nucleotide polymorphisms of complement component 5 and periodontitis
[PMID 31570557
] Association of TRAF1/C5 locus polymorphisms with epilepsy and clinical traits in Mexican neurocysticercosis patients.
