rs2428496
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common in complete genomics |
| (G;G) | 0 | common in clinvar |
| Make rs2428496(A;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 31354344 |
| Gene | HLA-B |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2428496 |
| dbSNP (classic) | rs2428496 |
| ClinGen | rs2428496 |
| ebi | rs2428496 |
| HLI | rs2428496 |
| Exac | rs2428496 |
| Gnomad | rs2428496 |
| Varsome | rs2428496 |
| LitVar | rs2428496 |
| Map | rs2428496 |
| PheGenI | rs2428496 |
| Biobank | rs2428496 |
| 1000 genomes | rs2428496 |
| hgdp | rs2428496 |
| ensembl | rs2428496 |
| geneview | rs2428496 |
| scholar | rs2428496 |
| rs2428496 | |
| pharmgkb | rs2428496 |
| gwascentral | rs2428496 |
| openSNP | rs2428496 |
| 23andMe | rs2428496 |
| SNPshot | rs2428496 |
| SNPdbe | rs2428496 |
| MSV3d | rs2428496 |
| GWAS Ctlg | rs2428496 |
| GMAF | 0.1841 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | Rs2428496(A;A) |
| Alt | Rs2428496(A;A) |
| Reference | Rs2428496(G;G) |
| Significance | Histocompatibility |
| Disease | |
| Variation | info |
| Gene | HLA-B |
| CLNDBN | |
| Reversed | 1 |
| HGVS | NC_000006.11:g.31322121C>T |
| CLNSRC | |
| CLNACC | |
