rs9266197
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs9266197(A;A) |
| Make rs9266197(A;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 31357053 |
| Gene | HLA-B, MIR6891 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs9266197 |
| dbSNP (classic) | rs9266197 |
| ClinGen | rs9266197 |
| ebi | rs9266197 |
| HLI | rs9266197 |
| Exac | rs9266197 |
| Gnomad | rs9266197 |
| Varsome | rs9266197 |
| LitVar | rs9266197 |
| Map | rs9266197 |
| PheGenI | rs9266197 |
| Biobank | rs9266197 |
| 1000 genomes | rs9266197 |
| hgdp | rs9266197 |
| ensembl | rs9266197 |
| geneview | rs9266197 |
| scholar | rs9266197 |
| rs9266197 | |
| pharmgkb | rs9266197 |
| gwascentral | rs9266197 |
| openSNP | rs9266197 |
| 23andMe | rs9266197 |
| SNPshot | rs9266197 |
| SNPdbe | rs9266197 |
| MSV3d | rs9266197 |
| GWAS Ctlg | rs9266197 |
| GMAF | 0.2819 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs9266197(A;A) |
| Alt | rs9266197(A;A) |
| Reference | Rs9266197(G;G) |
| Significance | Histocompatibility |
| Disease | |
| Variation | info |
| Gene | HLA-B |
| CLNDBN | |
| Reversed | 0 |
| HGVS | NC_000006.11:g.31324830G>A |
| CLNSRC | |
| CLNACC | |
