rs9276606
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs9276606(A;A) |
| Make rs9276606(A;T) |
| Make rs9276606(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 32768918 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs9276606 |
| dbSNP (classic) | rs9276606 |
| ClinGen | rs9276606 |
| ebi | rs9276606 |
| HLI | rs9276606 |
| Exac | rs9276606 |
| Gnomad | rs9276606 |
| Varsome | rs9276606 |
| LitVar | rs9276606 |
| Map | rs9276606 |
| PheGenI | rs9276606 |
| Biobank | rs9276606 |
| 1000 genomes | rs9276606 |
| hgdp | rs9276606 |
| ensembl | rs9276606 |
| geneview | rs9276606 |
| scholar | rs9276606 |
| rs9276606 | |
| pharmgkb | rs9276606 |
| gwascentral | rs9276606 |
| openSNP | rs9276606 |
| 23andMe | rs9276606 |
| SNPshot | rs9276606 |
| SNPdbe | rs9276606 |
| MSV3d | rs9276606 |
| GWAS Ctlg | rs9276606 |
| GMAF | 0.2039 |
| Max Magnitude | 0 |
| GWAS snp | |
|---|---|
| PMID | [PMID 23028341 ]
|
| Trait | Complement C3 and C4 levels |
| Title | Genome-wide association study for serum complement C3 and C4 levels in healthy Chinese subjects. |
| Risk Allele | T |
| P-val | 3E-22 |
| Odds Ratio | .09 [0.070-0.110] g/L decrease |
