rs121909560
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (AG;AG) | 0 | common in clinvar |
| Make rs121909560(-;-) |
| Make rs121909560(-;AG) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 173909737 |
| Gene | SERPINC1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs121909560 |
| dbSNP (classic) | rs121909560 |
| ClinGen | rs121909560 |
| ebi | rs121909560 |
| HLI | rs121909560 |
| Exac | rs121909560 |
| Gnomad | rs121909560 |
| Varsome | rs121909560 |
| LitVar | rs121909560 |
| Map | rs121909560 |
| PheGenI | rs121909560 |
| Biobank | rs121909560 |
| 1000 genomes | rs121909560 |
| hgdp | rs121909560 |
| ensembl | rs121909560 |
| geneview | rs121909560 |
| scholar | rs121909560 |
| rs121909560 | |
| pharmgkb | rs121909560 |
| gwascentral | rs121909560 |
| openSNP | rs121909560 |
| 23andMe | rs121909560 |
| SNPshot | rs121909560 |
| SNPdbe | rs121909560 |
| MSV3d | rs121909560 |
| GWAS Ctlg | rs121909560 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs121909560(-;-) |
| Alt | rs121909560(-;-) |
| Reference | Rs121909560(AG;AG) |
| Significance | Pathogenic |
| Disease | Antithrombin III deficiency |
| Variation | info |
| Gene | SERPINC1 |
| CLNDBN | Antithrombin III deficiency |
| Reversed | 1 |
| HGVS | NC_000001.10:g.173878875_173878876delCT |
| CLNSRC | OMIM Allelic Variant |
| CLNACC | RCV000019643.27, |
