rs61760866
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs61760866(-;-) |
| Make rs61760866(-;C) |
| Reference | GRCh37.p5 37.3/137 |
| Chromosome | 6 |
| Position | 29910739 |
| Gene | HLA-A |
| is a | snp |
| is | mentioned by |
| dbSNP | rs61760866 |
| dbSNP (classic) | rs61760866 |
| ClinGen | rs61760866 |
| ebi | rs61760866 |
| HLI | rs61760866 |
| Exac | rs61760866 |
| Gnomad | rs61760866 |
| Varsome | rs61760866 |
| LitVar | rs61760866 |
| Map | rs61760866 |
| PheGenI | rs61760866 |
| Biobank | rs61760866 |
| 1000 genomes | rs61760866 |
| hgdp | rs61760866 |
| ensembl | rs61760866 |
| geneview | rs61760866 |
| scholar | rs61760866 |
| rs61760866 | |
| pharmgkb | rs61760866 |
| gwascentral | rs61760866 |
| openSNP | rs61760866 |
| 23andMe | rs61760866 |
| SNPshot | rs61760866 |
| SNPdbe | rs61760866 |
| MSV3d | rs61760866 |
| GWAS Ctlg | rs61760866 |
| Status | Deleted |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | |
| Alt | |
| Reference | Rs61760866(C;C) |
| Significance | Histocompatibility |
| Disease | |
| Variation | info |
| Gene | HLA-A |
| CLNDBN | |
| Reversed | 0 |
| HGVS | NC_000006.11:g.29910739delC |
| CLNSRC | |
| CLNACC | |
