rs139850307
From SNPedia
| Merged into | rs1050556 |
| Orientation | minus |
| Stabilized | plus |
| Make rs139850307(C;C) |
| Make rs139850307(C;G) |
| Make rs139850307(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 31356809 |
| Gene | HLA-B |
| is a | snp |
| is | mentioned by |
| dbSNP | rs139850307 |
| dbSNP (classic) | rs139850307 |
| ClinGen | rs139850307 |
| ebi | rs139850307 |
| HLI | rs139850307 |
| Exac | rs139850307 |
| Gnomad | rs139850307 |
| Varsome | rs139850307 |
| LitVar | rs139850307 |
| Map | rs139850307 |
| PheGenI | rs139850307 |
| Biobank | rs139850307 |
| 1000 genomes | rs139850307 |
| hgdp | rs139850307 |
| ensembl | rs139850307 |
| geneview | rs139850307 |
| scholar | rs139850307 |
| rs139850307 | |
| pharmgkb | rs139850307 |
| gwascentral | rs139850307 |
| openSNP | rs139850307 |
| 23andMe | rs139850307 |
| SNPshot | rs139850307 |
| SNPdbe | rs139850307 |
| MSV3d | rs139850307 |
| GWAS Ctlg | rs139850307 |
| Status | Merged into rs1050556 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs139850307(T;T) |
| Alt | rs139850307(T;T) |
| Reference | rs139850307(C;C) |
| Significance | Histocompatibility |
| Disease | |
| Variation | info |
| Gene | HLA-B |
| CLNDBN | |
| Reversed | 0 |
| HGVS | NC_000006.11:g.31324586C>T |
| CLNSRC | |
| CLNACC | |
