rs151341178
From SNPedia
| Merged into | rs1065386 |
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs151341178(C;G) |
| Make rs151341178(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 31356770 |
| Gene | HLA-B |
| is a | snp |
| is | mentioned by |
| dbSNP | rs151341178 |
| dbSNP (classic) | rs151341178 |
| ClinGen | rs151341178 |
| ebi | rs151341178 |
| HLI | rs151341178 |
| Exac | rs151341178 |
| Gnomad | rs151341178 |
| Varsome | rs151341178 |
| LitVar | rs151341178 |
| Map | rs151341178 |
| PheGenI | rs151341178 |
| Biobank | rs151341178 |
| 1000 genomes | rs151341178 |
| hgdp | rs151341178 |
| ensembl | rs151341178 |
| geneview | rs151341178 |
| scholar | rs151341178 |
| rs151341178 | |
| pharmgkb | rs151341178 |
| gwascentral | rs151341178 |
| openSNP | rs151341178 |
| 23andMe | rs151341178 |
| SNPshot | rs151341178 |
| SNPdbe | rs151341178 |
| MSV3d | rs151341178 |
| GWAS Ctlg | rs151341178 |
| Status | Merged into rs1065386 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs151341178(G;G) |
| Alt | rs151341178(G;G) |
| Reference | Rs151341178(C;C) |
| Significance | Histocompatibility |
| Disease | |
| Variation | info |
| Gene | HLA-B |
| CLNDBN | |
| Reversed | 1 |
| HGVS | NC_000006.11:g.31324547G>C |
| CLNSRC | |
| CLNACC | |
