rs36209567
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs36209567(C;T) |
| Make rs36209567(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 13 |
| Position | 113118668 |
| Gene | F7 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs36209567 |
| dbSNP (classic) | rs36209567 |
| ClinGen | rs36209567 |
| ebi | rs36209567 |
| HLI | rs36209567 |
| Exac | rs36209567 |
| Gnomad | rs36209567 |
| Varsome | rs36209567 |
| LitVar | rs36209567 |
| Map | rs36209567 |
| PheGenI | rs36209567 |
| Biobank | rs36209567 |
| 1000 genomes | rs36209567 |
| hgdp | rs36209567 |
| ensembl | rs36209567 |
| geneview | rs36209567 |
| scholar | rs36209567 |
| rs36209567 | |
| pharmgkb | rs36209567 |
| gwascentral | rs36209567 |
| openSNP | rs36209567 |
| 23andMe | rs36209567 |
| SNPshot | rs36209567 |
| SNPdbe | rs36209567 |
| MSV3d | rs36209567 |
| GWAS Ctlg | rs36209567 |
| GMAF | 0.0009183 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs36209567(T;T) |
| Alt | rs36209567(T;T) |
| Reference | Rs36209567(C;C) |
| Significance | Pathogenic |
| Disease | Factor VII deficiency |
| Variation | info |
| Gene | F7 |
| CLNDBN | Factor VII deficiency |
| Reversed | 0 |
| HGVS | NC_000013.10:g.113772982C>T |
| CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
| CLNACC | RCV000012857.3, |
