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 |
|---|---|---|---|---|---|
| 0 | 0 | 22 | 8 | 6 | 32 |
Condition and significance breakdown #
Total conditions: 4
| Condition | uncertain significance | likely benign | benign | total |
|---|---|---|---|---|
| Inborn genetic diseases | 21 | 3 | 0 | 24 |
| not provided | 0 | 4 | 6 | 8 |
| Neurofibromatosis, type 1 | 0 | 1 | 1 | 1 |
| not specified | 1 | 0 | 0 | 1 |
Submitter and significance breakdown #
Total submitters: 6
| Submitter | uncertain significance | likely benign | benign | total |
|---|---|---|---|---|
| Ambry Genetics | 21 | 3 | 0 | 24 |
| CeGaT Center for Human Genetics Tuebingen | 0 | 2 | 3 | 5 |
| Center for Pediatric Genomic Medicine, Children's Mercy Hospital and Clinics | 0 | 1 | 2 | 3 |
| Invitae | 0 | 1 | 1 | 2 |
| Mendelics | 1 | 1 | 0 | 2 |
| Genome-Nilou Lab | 0 | 0 | 1 | 1 |