rs750046020
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs750046020(C;G) |
| Make rs750046020(G;G) |
| Reference | GRCh38.p7 38.3/149 |
| Chromosome | 1 |
| Position | 43338646 |
| Gene | MPL |
| is a | snp |
| is | mentioned by |
| dbSNP | rs750046020 |
| dbSNP (classic) | rs750046020 |
| ClinGen | rs750046020 |
| ebi | rs750046020 |
| HLI | rs750046020 |
| Exac | rs750046020 |
| Gnomad | rs750046020 |
| Varsome | rs750046020 |
| LitVar | rs750046020 |
| Map | rs750046020 |
| PheGenI | rs750046020 |
| Biobank | rs750046020 |
| 1000 genomes | rs750046020 |
| hgdp | rs750046020 |
| ensembl | rs750046020 |
| geneview | rs750046020 |
| scholar | rs750046020 |
| rs750046020 | |
| pharmgkb | rs750046020 |
| gwascentral | rs750046020 |
| openSNP | rs750046020 |
| 23andMe | rs750046020 |
| SNPshot | rs750046020 |
| SNPdbe | rs750046020 |
| MSV3d | rs750046020 |
| GWAS Ctlg | rs750046020 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs750046020(G;G) rs750046020(T;T) |
| Alt | rs750046020(G;G) rs750046020(T;T) |
| Reference | Rs750046020(C;C) |
| Significance | Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | MPL |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000001.10:g.43804317C>T |
| CLNSRC | |
| CLNACC | RCV000255329.1, |
