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 |
|---|---|---|---|---|---|
| 16 | 6 | 231 | 117 | 24 | 382 |
Gene and significance breakdown #
Total genes and gene combinations: 1
| Gene or gene combination | pathogenic | likely pathogenic | uncertain significance | likely benign | benign | total |
|---|---|---|---|---|---|---|
| CEP41 | 16 | 6 | 231 | 117 | 24 | 382 |
Submitter and significance breakdown #
Total submitters: 12
| Submitter | pathogenic | likely pathogenic | uncertain significance | likely benign | benign | total |
|---|---|---|---|---|---|---|
| Labcorp Genetics (formerly Invitae), Labcorp | 10 | 3 | 140 | 105 | 8 | 266 |
| Illumina Laboratory Services, Illumina | 0 | 0 | 95 | 13 | 16 | 124 |
| Department of Pathology and Laboratory Medicine, Sinai Health System | 0 | 0 | 5 | 0 | 0 | 5 |
| Fulgent Genetics, Fulgent Genetics | 0 | 1 | 4 | 0 | 0 | 5 |
| OMIM | 4 | 0 | 0 | 0 | 0 | 4 |
| Baylor Genetics | 1 | 0 | 2 | 0 | 0 | 3 |
| Joe DiMaggio Children's Hospital, Memorial Healthcare System | 2 | 0 | 0 | 0 | 0 | 2 |
| Rady Children's Institute for Genomic Medicine, Rady Children's Hospital San Diego | 1 | 1 | 0 | 0 | 0 | 2 |
| Genome-Nilou Lab | 0 | 0 | 0 | 0 | 1 | 1 |
| Neuberg Centre For Genomic Medicine, NCGM | 0 | 1 | 0 | 0 | 0 | 1 |
| Revvity Omics, Revvity | 0 | 0 | 1 | 0 | 0 | 1 |
| Victorian Clinical Genetics Services, Murdoch Childrens Research Institute | 0 | 0 | 1 | 0 | 0 | 1 |