rs148434485
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs148434485(C;T) |
| Make rs148434485(T;T) |
| Reference | GRCh38.p7 38.3/150 |
| Chromosome | 1 |
| Position | 43338146 |
| Gene | MPL |
| is a | snp |
| is | mentioned by |
| dbSNP | rs148434485 |
| dbSNP (classic) | rs148434485 |
| ClinGen | rs148434485 |
| ebi | rs148434485 |
| HLI | rs148434485 |
| Exac | rs148434485 |
| Gnomad | rs148434485 |
| Varsome | rs148434485 |
| LitVar | rs148434485 |
| Map | rs148434485 |
| PheGenI | rs148434485 |
| Biobank | rs148434485 |
| 1000 genomes | rs148434485 |
| hgdp | rs148434485 |
| ensembl | rs148434485 |
| geneview | rs148434485 |
| scholar | rs148434485 |
| rs148434485 | |
| pharmgkb | rs148434485 |
| gwascentral | rs148434485 |
| openSNP | rs148434485 |
| 23andMe | rs148434485 |
| SNPshot | rs148434485 |
| SNPdbe | rs148434485 |
| MSV3d | rs148434485 |
| GWAS Ctlg | rs148434485 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs148434485(T;T) |
| Alt | rs148434485(T;T) |
| Reference | Rs148434485(C;C) |
| Significance | Pathogenic |
| Disease | Congenital amegakaryocytic thrombocytopenia |
| Variation | info |
| Gene | MPL |
| CLNDBN | Congenital amegakaryocytic thrombocytopenia |
| Reversed | 0 |
| HGVS | NC_000001.10:g.43803817C>T |
| CLNSRC | |
| CLNACC | RCV000411190.1, |
