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 | risk factor | total |
|---|---|---|---|---|---|---|
| 2 | 0 | 4 | 0 | 0 | 3 | 9 |
Gene and significance breakdown #
Total genes and gene combinations: 1
| Gene or gene combination | pathogenic | uncertain significance | risk factor | total |
|---|---|---|---|---|
| HCN2 | 2 | 4 | 3 | 9 |
Submitter and significance breakdown #
Total submitters: 5
| Submitter | pathogenic | uncertain significance | risk factor | total |
|---|---|---|---|---|
| OMIM | 2 | 0 | 3 | 5 |
| Institute of Human Genetics, University of Leipzig Medical Center | 0 | 1 | 0 | 1 |
| Institute of Human Genetics, Clinical Exome/Genome Diagnostics Group, University Hospital Bonn | 0 | 1 | 0 | 1 |
| Neuberg Centre For Genomic Medicine, NCGM | 0 | 1 | 0 | 1 |
| Laboratorio de Genetica e Diagnostico Molecular, Hospital Israelita Albert Einstein | 0 | 1 | 0 | 1 |