rs2277984
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs2277984(A;A) |
| Make rs2277984(A;G) |
| Reference | GRCh38.p2 38.2/144 |
| Chromosome | 19 |
| Position | 6679500 |
| Gene | C3 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2277984 |
| dbSNP (classic) | rs2277984 |
| ClinGen | rs2277984 |
| ebi | rs2277984 |
| HLI | rs2277984 |
| Exac | rs2277984 |
| Gnomad | rs2277984 |
| Varsome | rs2277984 |
| LitVar | rs2277984 |
| Map | rs2277984 |
| PheGenI | rs2277984 |
| Biobank | rs2277984 |
| 1000 genomes | rs2277984 |
| hgdp | rs2277984 |
| ensembl | rs2277984 |
| geneview | rs2277984 |
| scholar | rs2277984 |
| rs2277984 | |
| pharmgkb | rs2277984 |
| gwascentral | rs2277984 |
| openSNP | rs2277984 |
| 23andMe | rs2277984 |
| SNPshot | rs2277984 |
| SNPdbe | rs2277984 |
| MSV3d | rs2277984 |
| GWAS Ctlg | rs2277984 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 26503818] Complement 3 and metabolic syndrome induced by clozapine: a cross-sectional study and retrospective cohort analysis
| ClinVar | |
|---|---|
| Risk | rs2277984(A;A) |
| Alt | rs2277984(A;A) |
| Reference | Rs2277984(G;G) |
| Significance | Non-pathogenic |
| Disease | Macular degeneration C3 deficiency Atypical hemolytic uremic syndrome |
| Variation | info |
| Gene | C3 |
| CLNDBN | Macular degeneration C3 deficiency Atypical hemolytic uremic syndrome |
| Reversed | 1 |
| HGVS | NC_000019.9:g.6679511C>T |
| CLNSRC | |
| CLNACC | RCV000261116.1, RCV000316465.1, RCV000389627.1, |
