rs1063499
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs1063499(C;C) |
| Make rs1063499(C;G) |
| Make rs1063499(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 5 |
| Position | 40955459 |
| Gene | C7 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1063499 |
| dbSNP (classic) | rs1063499 |
| ClinGen | rs1063499 |
| ebi | rs1063499 |
| HLI | rs1063499 |
| Exac | rs1063499 |
| Gnomad | rs1063499 |
| Varsome | rs1063499 |
| LitVar | rs1063499 |
| Map | rs1063499 |
| PheGenI | rs1063499 |
| Biobank | rs1063499 |
| 1000 genomes | rs1063499 |
| hgdp | rs1063499 |
| ensembl | rs1063499 |
| geneview | rs1063499 |
| scholar | rs1063499 |
| rs1063499 | |
| pharmgkb | rs1063499 |
| gwascentral | rs1063499 |
| openSNP | rs1063499 |
| 23andMe | rs1063499 |
| SNPshot | rs1063499 |
| SNPdbe | rs1063499 |
| MSV3d | rs1063499 |
| GWAS Ctlg | rs1063499 |
| GMAF | 0.4894 |
| Max Magnitude | 0 |
| ? | (C;C) (C;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 19221116
] Use of a genetic isolate to identify rare disease variants: C7 on 5p associated with MS.
[PMID 19344414] Risk of non-Hodgkin lymphoma in association with germline variation in complement genes.
