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 | not provided | total |
|---|---|---|---|---|---|---|
| 3 | 5 | 5 | 2 | 0 | 2 | 15 |
Gene and significance breakdown #
Total genes and gene combinations: 3
| Gene or gene combination | pathogenic | likely pathogenic | uncertain significance | likely benign | not provided | total |
|---|---|---|---|---|---|---|
| WNT10A | 3 | 5 | 3 | 2 | 2 | 13 |
| LOC129935618, WNT10A | 0 | 0 | 1 | 0 | 0 | 1 |
| LOC129935619, WNT10A | 0 | 0 | 1 | 0 | 0 | 1 |
Submitter and significance breakdown #
Total submitters: 5
| Submitter | pathogenic | likely pathogenic | uncertain significance | likely benign | not provided | total |
|---|---|---|---|---|---|---|
| Fulgent Genetics, Fulgent Genetics | 2 | 4 | 5 | 2 | 0 | 13 |
| Division of Human Genetics, Children's Hospital of Philadelphia | 1 | 1 | 0 | 0 | 0 | 2 |
| GenomeConnect - Invitae Patient Insights Network | 0 | 0 | 0 | 0 | 2 | 2 |
| New York Genome Center | 1 | 0 | 0 | 0 | 0 | 1 |
| GenomeConnect - Brain Gene Registry | 0 | 0 | 0 | 0 | 1 | 1 |