rs144857500
From SNPedia
| Merged into | rs1050543 |
| Orientation | minus |
| Stabilized | plus |
| Make rs144857500(C;C) |
| Make rs144857500(C;G) |
| Make rs144857500(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 31356818 |
| Gene | HLA-B |
| is a | snp |
| is | mentioned by |
| dbSNP | rs144857500 |
| dbSNP (classic) | rs144857500 |
| ClinGen | rs144857500 |
| ebi | rs144857500 |
| HLI | rs144857500 |
| Exac | rs144857500 |
| Gnomad | rs144857500 |
| Varsome | rs144857500 |
| LitVar | rs144857500 |
| Map | rs144857500 |
| PheGenI | rs144857500 |
| Biobank | rs144857500 |
| 1000 genomes | rs144857500 |
| hgdp | rs144857500 |
| ensembl | rs144857500 |
| geneview | rs144857500 |
| scholar | rs144857500 |
| rs144857500 | |
| pharmgkb | rs144857500 |
| gwascentral | rs144857500 |
| openSNP | rs144857500 |
| 23andMe | rs144857500 |
| SNPshot | rs144857500 |
| SNPdbe | rs144857500 |
| MSV3d | rs144857500 |
| GWAS Ctlg | rs144857500 |
| Status | Merged into rs1050543 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs144857500(G;G) |
| Alt | rs144857500(G;G) |
| Reference | rs144857500(C;C) |
| Significance | Histocompatibility |
| Disease | |
| Variation | info |
| Gene | HLA-B |
| CLNDBN | |
| Reversed | 0 |
| HGVS | NC_000006.11:g.31324595C>G |
| CLNSRC | |
| CLNACC | |
