rs16899066
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in clinvar |
| Make rs16899066(C;C) |
| Make rs16899066(C;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 31355803 |
| Gene | HLA-B, MIR6891 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs16899066 |
| dbSNP (classic) | rs16899066 |
| ClinGen | rs16899066 |
| ebi | rs16899066 |
| HLI | rs16899066 |
| Exac | rs16899066 |
| Gnomad | rs16899066 |
| Varsome | rs16899066 |
| LitVar | rs16899066 |
| Map | rs16899066 |
| PheGenI | rs16899066 |
| Biobank | rs16899066 |
| 1000 genomes | rs16899066 |
| hgdp | rs16899066 |
| ensembl | rs16899066 |
| geneview | rs16899066 |
| scholar | rs16899066 |
| rs16899066 | |
| pharmgkb | rs16899066 |
| gwascentral | rs16899066 |
| openSNP | rs16899066 |
| 23andMe | rs16899066 |
| SNPshot | rs16899066 |
| SNPdbe | rs16899066 |
| MSV3d | rs16899066 |
| GWAS Ctlg | rs16899066 |
| GMAF | 0.01699 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs16899066(C;C) |
| Alt | rs16899066(C;C) |
| Reference | Rs16899066(T;T) |
| Significance | Histocompatibility |
| Disease | |
| Variation | info |
| Gene | HLA-B |
| CLNDBN | |
| Reversed | 0 |
| HGVS | NC_000006.11:g.31323580T>C |
| CLNSRC | |
| CLNACC | |
