rs137852248
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| (C;T) | 3.5 | Carrier of a Hemophilia B mutation |
| (T;T) | 5.5 | Hemophilia B (severity varies) |
| Reference | GRCh38 38.1/141 |
| Chromosome | X |
| Position | 139561565 |
| Gene | F9 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs137852248 |
| dbSNP (classic) | rs137852248 |
| ClinGen | rs137852248 |
| ebi | rs137852248 |
| HLI | rs137852248 |
| Exac | rs137852248 |
| Gnomad | rs137852248 |
| Varsome | rs137852248 |
| LitVar | rs137852248 |
| Map | rs137852248 |
| PheGenI | rs137852248 |
| Biobank | rs137852248 |
| 1000 genomes | rs137852248 |
| hgdp | rs137852248 |
| ensembl | rs137852248 |
| geneview | rs137852248 |
| scholar | rs137852248 |
| rs137852248 | |
| pharmgkb | rs137852248 |
| gwascentral | rs137852248 |
| openSNP | rs137852248 |
| 23andMe | rs137852248 |
| SNPshot | rs137852248 |
| SNPdbe | rs137852248 |
| MSV3d | rs137852248 |
| GWAS Ctlg | rs137852248 |
| Max Magnitude | 5.5 |
| ClinVar | |
|---|---|
| Risk | Rs137852248(T;T) |
| Alt | Rs137852248(T;T) |
| Reference | Rs137852248(C;C) |
| Significance | Pathogenic |
| Disease | Hereditary factor IX deficiency disease |
| Variation | info |
| Gene | F9 |
| CLNDBN | Hereditary factor IX deficiency disease |
| Reversed | 0 |
| HGVS | NC_000023.10:g.138643724C>T |
| CLNSRC | OMIM Allelic Variant |
| CLNACC | RCV000011333.7, |
