rs45611338
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in clinvar |
| Make rs45611338(-;-) |
| Make rs45611338(-;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 31355892 |
| Gene | HLA-B, MIR6891 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs45611338 |
| dbSNP (classic) | rs45611338 |
| ClinGen | rs45611338 |
| ebi | rs45611338 |
| HLI | rs45611338 |
| Exac | rs45611338 |
| Gnomad | rs45611338 |
| Varsome | rs45611338 |
| LitVar | rs45611338 |
| Map | rs45611338 |
| PheGenI | rs45611338 |
| Biobank | rs45611338 |
| 1000 genomes | rs45611338 |
| hgdp | rs45611338 |
| ensembl | rs45611338 |
| geneview | rs45611338 |
| scholar | rs45611338 |
| rs45611338 | |
| pharmgkb | rs45611338 |
| gwascentral | rs45611338 |
| openSNP | rs45611338 |
| 23andMe | rs45611338 |
| SNPshot | rs45611338 |
| SNPdbe | rs45611338 |
| MSV3d | rs45611338 |
| GWAS Ctlg | rs45611338 |
| GMAF | 0.01745 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | |
| Alt | |
| Reference | Rs45611338(T;T) |
| Significance | Histocompatibility |
| Disease | |
| Variation | info |
| Gene | HLA-B |
| CLNDBN | |
| Reversed | 1 |
| HGVS | NC_000006.11:g.31323672delA |
| CLNSRC | |
| CLNACC | |
