rs2227598
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs2227598(C;C) |
| Make rs2227598(C;T) |
| Make rs2227598(T;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 1 |
| Position | 173915033 |
| Gene | SERPINC1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2227598 |
| dbSNP (classic) | rs2227598 |
| ClinGen | rs2227598 |
| ebi | rs2227598 |
| HLI | rs2227598 |
| Exac | rs2227598 |
| Gnomad | rs2227598 |
| Varsome | rs2227598 |
| LitVar | rs2227598 |
| Map | rs2227598 |
| PheGenI | rs2227598 |
| Biobank | rs2227598 |
| 1000 genomes | rs2227598 |
| hgdp | rs2227598 |
| ensembl | rs2227598 |
| geneview | rs2227598 |
| scholar | rs2227598 |
| rs2227598 | |
| pharmgkb | rs2227598 |
| gwascentral | rs2227598 |
| openSNP | rs2227598 |
| 23andMe | rs2227598 |
| SNPshot | rs2227598 |
| SNPdbe | rs2227598 |
| MSV3d | rs2227598 |
| GWAS Ctlg | rs2227598 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 25811371
] Antithrombin III Deficiency in Indian Patients with Deep Vein Thrombosis: Identification of First India Based AT Variants Including a Novel Point Mutation (T280A) that Leads to Aggregation
