If a variant has more than one submission, it may be counted in more than one significance column. If this is the case, the total number of variants will be less than the sum of the other cells.
| pathogenic | likely pathogenic | uncertain significance | likely benign | benign | total |
|---|---|---|---|---|---|
| 38 | 21 | 21 | 0 | 3 | 82 |
Gene and significance breakdown #
Total genes and gene combinations: 5
| Gene or gene combination | pathogenic | likely pathogenic | uncertain significance | benign | total |
|---|---|---|---|---|---|
| ITGA2B | 33 | 15 | 18 | 3 | 68 |
| ITGB3 | 2 | 5 | 0 | 0 | 7 |
| EFCAB13-DT, ITGB3 | 1 | 0 | 2 | 0 | 3 |
| ITGA2B, LOC130060983 | 2 | 0 | 1 | 0 | 3 |
| ITGB3, LOC130061044 | 0 | 1 | 0 | 0 | 1 |
Submitter and significance breakdown #
Total submitters: 12
| Submitter | pathogenic | likely pathogenic | uncertain significance | benign | total |
|---|---|---|---|---|---|
| ISTH-SSC Genomics in Thrombosis and Hemostasis, KU Leuven, Center for Molecular and Vascular Biology | 19 | 14 | 12 | 0 | 45 |
| OMIM | 14 | 0 | 0 | 0 | 14 |
| Women's Health and Genetics/Laboratory Corporation of America, LabCorp | 0 | 5 | 0 | 0 | 5 |
| 3billion | 2 | 0 | 3 | 0 | 5 |
| Neuberg Centre For Genomic Medicine, NCGM | 3 | 1 | 1 | 0 | 5 |
| Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center | 1 | 1 | 2 | 0 | 4 |
| Genome-Nilou Lab | 0 | 0 | 0 | 3 | 3 |
| Genetics and Molecular Pathology, SA Pathology | 1 | 0 | 1 | 0 | 2 |
| KardioGenetik, Herz- und Diabeteszentrum NRW | 1 | 0 | 1 | 0 | 2 |
| Baylor Genetics | 1 | 0 | 0 | 0 | 1 |
| Unidade de Genética Molecular, Centro Hospitalar Universitário do Porto | 0 | 0 | 1 | 0 | 1 |
| Palindrome, Gene Kavoshgaran Aria | 1 | 0 | 0 | 0 | 1 |