rs2596497
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in complete genomics |
| (T;T) | 0 | common in clinvar |
| Make rs2596497(C;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 31354927 |
| Gene | HLA-B, MIR6891 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2596497 |
| dbSNP (classic) | rs2596497 |
| ClinGen | rs2596497 |
| ebi | rs2596497 |
| HLI | rs2596497 |
| Exac | rs2596497 |
| Gnomad | rs2596497 |
| Varsome | rs2596497 |
| LitVar | rs2596497 |
| Map | rs2596497 |
| PheGenI | rs2596497 |
| Biobank | rs2596497 |
| 1000 genomes | rs2596497 |
| hgdp | rs2596497 |
| ensembl | rs2596497 |
| geneview | rs2596497 |
| scholar | rs2596497 |
| rs2596497 | |
| pharmgkb | rs2596497 |
| gwascentral | rs2596497 |
| openSNP | rs2596497 |
| 23andMe | rs2596497 |
| SNPshot | rs2596497 |
| SNPdbe | rs2596497 |
| MSV3d | rs2596497 |
| GWAS Ctlg | rs2596497 |
| GMAF | 0.1538 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | Rs2596497(C;C) |
| Alt | Rs2596497(C;C) |
| Reference | Rs2596497(T;T) |
| Significance | Histocompatibility |
| Disease | |
| Variation | info |
| Gene | HLA-B |
| CLNDBN | |
| Reversed | 1 |
| HGVS | NC_000006.11:g.31322704A>G |
| CLNSRC | |
| CLNACC | |
