rs1050696
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in clinvar |
| Make rs1050696(C;C) |
| Make rs1050696(C;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 31356203 |
| Gene | HLA-B, MIR6891 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1050696 |
| dbSNP (classic) | rs1050696 |
| ClinGen | rs1050696 |
| ebi | rs1050696 |
| HLI | rs1050696 |
| Exac | rs1050696 |
| Gnomad | rs1050696 |
| Varsome | rs1050696 |
| LitVar | rs1050696 |
| Map | rs1050696 |
| PheGenI | rs1050696 |
| Biobank | rs1050696 |
| 1000 genomes | rs1050696 |
| hgdp | rs1050696 |
| ensembl | rs1050696 |
| geneview | rs1050696 |
| scholar | rs1050696 |
| rs1050696 | |
| pharmgkb | rs1050696 |
| gwascentral | rs1050696 |
| openSNP | rs1050696 |
| 23andMe | rs1050696 |
| SNPshot | rs1050696 |
| SNPdbe | rs1050696 |
| MSV3d | rs1050696 |
| GWAS Ctlg | rs1050696 |
| GMAF | 0.08907 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs1050696(C;C) |
| Alt | rs1050696(C;C) |
| Reference | Rs1050696(T;T) |
| Significance | Histocompatibility |
| Disease | |
| Variation | info |
| Gene | HLA-B |
| CLNDBN | |
| Reversed | 1 |
| HGVS | NC_000006.11:g.31323980A>G |
| CLNSRC | |
| CLNACC | |
