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 |
---|---|---|---|---|---|---|
10 | 1 | 11 | 6 | 1 | 1 | 30 |
Gene and significance breakdown #
Submitter and significance breakdown #
Submitter | pathogenic | likely pathogenic | uncertain significance | likely benign | benign | not provided | total |
---|---|---|---|---|---|---|---|
Fulgent Genetics, Fulgent Genetics | 0 | 0 | 0 | 5 | 1 | 0 | 6 |
Illumina Laboratory Services, Illumina | 0 | 0 | 5 | 1 | 0 | 0 | 6 |
Baylor Genetics | 4 | 0 | 0 | 0 | 0 | 0 | 4 |
Institute for Genomic Medicine (IGM) Clinical Laboratory, Nationwide Children's Hospital | 3 | 0 | 0 | 0 | 0 | 0 | 3 |
Centre for Mendelian Genomics, University Medical Centre Ljubljana | 0 | 0 | 2 | 0 | 0 | 0 | 2 |
MGZ Medical Genetics Center | 0 | 1 | 0 | 0 | 0 | 0 | 1 |
Mayo Clinic Laboratories, Mayo Clinic | 1 | 0 | 0 | 0 | 0 | 0 | 1 |
Service de Génétique Moléculaire, Hôpital Robert Debré | 0 | 0 | 1 | 0 | 0 | 0 | 1 |
Equipe Genetique des Anomalies du Developpement, Université de Bourgogne | 1 | 0 | 0 | 0 | 0 | 0 | 1 |
Institute of Human Genetics, University of Leipzig Medical Center | 0 | 0 | 1 | 0 | 0 | 0 | 1 |
GenomeConnect, ClinGen | 0 | 0 | 0 | 0 | 0 | 1 | 1 |
Genomic Medicine Lab, University of California San Francisco | 0 | 0 | 1 | 0 | 0 | 0 | 1 |
New York Genome Center | 0 | 0 | 1 | 0 | 0 | 0 | 1 |
Pediatrics, Sichuan Provincial Hospital For Women And Children | 1 | 0 | 0 | 0 | 0 | 0 | 1 |