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 |
|---|---|---|---|---|---|
| 10 | 4 | 9 | 0 | 5 | 27 |
Gene and significance breakdown #
Total genes and gene combinations: 1
| Gene or gene combination | pathogenic | likely pathogenic | uncertain significance | benign | total |
|---|---|---|---|---|---|
| FLVCR2 | 10 | 4 | 9 | 5 | 27 |
Submitter and significance breakdown #
Total submitters: 11
| Submitter | pathogenic | likely pathogenic | uncertain significance | benign | total |
|---|---|---|---|---|---|
| OMIM | 9 | 0 | 0 | 0 | 9 |
| Illumina Laboratory Services, Illumina | 0 | 0 | 4 | 2 | 6 |
| Genome-Nilou Lab | 0 | 0 | 0 | 3 | 3 |
| Genomic Medicine Center of Excellence, King Faisal Specialist Hospital and Research Centre | 1 | 1 | 1 | 0 | 2 |
| Faculty of Engineering and Natural Sciences, Biruni University | 0 | 1 | 1 | 0 | 2 |
| Baylor Genetics | 0 | 0 | 1 | 0 | 1 |
| Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine | 0 | 1 | 0 | 0 | 1 |
| Revvity Omics, Revvity | 0 | 0 | 1 | 0 | 1 |
| Department Of Genetics, Sultan Qaboos University Hospital, Sultan Qaboos University | 0 | 0 | 1 | 0 | 1 |
| Neuberg Centre For Genomic Medicine, NCGM | 0 | 0 | 1 | 0 | 1 |
| Breakthrough Genomics, Breakthrough Genomics | 0 | 1 | 0 | 0 | 1 |