rs137852748
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| (C;T) | 6.2 | Pulmonary arterial hypertension |
| Make rs137852748(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 2 |
| Position | 202556282 |
| Gene | BMPR2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs137852748 |
| dbSNP (classic) | rs137852748 |
| ClinGen | rs137852748 |
| ebi | rs137852748 |
| HLI | rs137852748 |
| Exac | rs137852748 |
| Gnomad | rs137852748 |
| Varsome | rs137852748 |
| LitVar | rs137852748 |
| Map | rs137852748 |
| PheGenI | rs137852748 |
| Biobank | rs137852748 |
| 1000 genomes | rs137852748 |
| hgdp | rs137852748 |
| ensembl | rs137852748 |
| geneview | rs137852748 |
| scholar | rs137852748 |
| rs137852748 | |
| pharmgkb | rs137852748 |
| gwascentral | rs137852748 |
| openSNP | rs137852748 |
| 23andMe | rs137852748 |
| SNPshot | rs137852748 |
| SNPdbe | rs137852748 |
| MSV3d | rs137852748 |
| GWAS Ctlg | rs137852748 |
| Max Magnitude | 6.2 |
aka c.2617C>T (p.Arg873Ter)
23andMe name: i5005634
| ClinVar | |
|---|---|
| Risk | rs137852748(T;T) |
| Alt | rs137852748(T;T) |
| Reference | Rs137852748(C;C) |
| Significance | Pathogenic |
| Disease | Primary pulmonary hypertension |
| Variation | info |
| Gene | BMPR2 |
| CLNDBN | Primary pulmonary hypertension |
| Reversed | 0 |
| HGVS | NC_000002.11:g.203421005C>T |
| CLNSRC | OMIM Allelic Variant |
| CLNACC | RCV000009350.3, |
