rs28934590
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in complete genomics |
| Make rs28934590(C;T) |
| Make rs28934590(T;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 6 |
| Position | 31933876 |
| Gene | C2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs28934590 |
| dbSNP (classic) | rs28934590 |
| ClinGen | rs28934590 |
| ebi | rs28934590 |
| HLI | rs28934590 |
| Exac | rs28934590 |
| Gnomad | rs28934590 |
| Varsome | rs28934590 |
| LitVar | rs28934590 |
| Map | rs28934590 |
| PheGenI | rs28934590 |
| Biobank | rs28934590 |
| 1000 genomes | rs28934590 |
| hgdp | rs28934590 |
| ensembl | rs28934590 |
| geneview | rs28934590 |
| scholar | rs28934590 |
| rs28934590 | |
| pharmgkb | rs28934590 |
| gwascentral | rs28934590 |
| openSNP | rs28934590 |
| 23andMe | rs28934590 |
| SNPshot | rs28934590 |
| SNPdbe | rs28934590 |
| MSV3d | rs28934590 |
| GWAS Ctlg | rs28934590 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs28934590(T;T) |
| Alt | rs28934590(T;T) |
| Reference | Rs28934590(C;C) |
| Significance | Untested |
| Disease | |
| Variation | info |
| Gene | C2 |
| CLNDBN | |
| Reversed | 0 |
| HGVS | NC_000006.11:g.31901653C>T |
| CLNSRC | |
| CLNACC | |
