rs45504795
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs45504795(-;-) |
| Make rs45504795(-;C) |
| Reference | GRCh37.p5 37.3/137 |
| Chromosome | 6 |
| Position | 31324371 |
| Gene | HLA-B |
| is a | snp |
| is | mentioned by |
| dbSNP | rs45504795 |
| dbSNP (classic) | rs45504795 |
| ClinGen | rs45504795 |
| ebi | rs45504795 |
| HLI | rs45504795 |
| Exac | rs45504795 |
| Gnomad | rs45504795 |
| Varsome | rs45504795 |
| LitVar | rs45504795 |
| Map | rs45504795 |
| PheGenI | rs45504795 |
| Biobank | rs45504795 |
| 1000 genomes | rs45504795 |
| hgdp | rs45504795 |
| ensembl | rs45504795 |
| geneview | rs45504795 |
| scholar | rs45504795 |
| rs45504795 | |
| pharmgkb | rs45504795 |
| gwascentral | rs45504795 |
| openSNP | rs45504795 |
| 23andMe | rs45504795 |
| SNPshot | rs45504795 |
| SNPdbe | rs45504795 |
| MSV3d | rs45504795 |
| GWAS Ctlg | rs45504795 |
| Status | Deleted |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | |
| Alt | |
| Reference | Rs45504795(C;C) |
| Significance | Histocompatibility |
| Disease | |
| Variation | info |
| Gene | HLA-B |
| CLNDBN | |
| Reversed | 1 |
| HGVS | NC_000006.11:g.31324371delG |
| CLNSRC | |
| CLNACC | |
