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 |
|---|---|---|---|---|---|
| 7 | 2 | 3 | 0 | 9 | 21 |
Gene and significance breakdown #
Total genes and gene combinations: 2
| Gene or gene combination | pathogenic | likely pathogenic | uncertain significance | benign | total |
|---|---|---|---|---|---|
| FLT4 | 7 | 2 | 3 | 8 | 20 |
| FLT4, LOC126807632 | 0 | 0 | 0 | 1 | 1 |
Submitter and significance breakdown #
Total submitters: 8
| Submitter | pathogenic | likely pathogenic | uncertain significance | benign | total |
|---|---|---|---|---|---|
| Genome-Nilou Lab | 0 | 0 | 0 | 9 | 9 |
| OMIM | 5 | 0 | 0 | 0 | 5 |
| Victorian Clinical Genetics Services, Murdoch Childrens Research Institute | 1 | 0 | 1 | 0 | 2 |
| Institute of Human Genetics, University of Goettingen | 0 | 0 | 1 | 0 | 1 |
| Molecular Genetics Department, Kulakov National Medical Research Center for Obstetrics, Gynecology and Perinatology | 0 | 1 | 0 | 0 | 1 |
| Institute of Human Genetics, University of Leipzig Medical Center | 0 | 1 | 0 | 0 | 1 |
| Rajaie Cardiovascular, Medical and Research Center, Iran University of Medical Sciences | 1 | 0 | 0 | 0 | 1 |
| Molecular Genetics Lab, CHRU Brest | 0 | 0 | 1 | 0 | 1 |