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 |
|---|---|---|---|---|---|
| 389 | 171 | 680 | 1945 | 152 | 3283 |
Gene and significance breakdown #
Total genes and gene combinations: 8
| Gene or gene combination | pathogenic | likely pathogenic | uncertain significance | likely benign | benign | total |
|---|---|---|---|---|---|---|
| EVC2 | 199 | 88 | 415 | 961 | 73 | 1706 |
| EVC | 163 | 71 | 215 | 903 | 68 | 1398 |
| EVC2, LOC126806961 | 11 | 6 | 43 | 63 | 11 | 132 |
| EVC2, LOC126806962 | 0 | 1 | 5 | 12 | 0 | 18 |
| EVC, LOC129992144 | 5 | 5 | 1 | 6 | 0 | 17 |
| EVC, EVC2 | 9 | 0 | 1 | 0 | 0 | 10 |
| ADD1, ADRA2C, CYTL1, DOK7, EVC2, FAM193A, GRK4, HAUS3, HGFAC, HTT, LINC01587, LRPAP1, LYAR, MSANTD1, MSX1, MXD4, NOP14, NSG1, OTOP1, POLN, RGS12, RNF4, SH3BP2, SLC75A1, STK32B, STX18, TMEM128, TNIP2, ZBTB49, ZFYVE28 | 1 | 0 | 0 | 0 | 0 | 1 |
| EVC2, LINC01587, STK32B | 1 | 0 | 0 | 0 | 0 | 1 |
Submitter and significance breakdown #
Total submitters: 7
| Submitter | pathogenic | likely pathogenic | uncertain significance | likely benign | benign | total |
|---|---|---|---|---|---|---|
| Labcorp Genetics (formerly Invitae), Labcorp | 387 | 99 | 658 | 1936 | 151 | 3231 |
| Fulgent Genetics, Fulgent Genetics | 23 | 82 | 23 | 8 | 3 | 139 |
| Department of Pathology and Laboratory Medicine, Sinai Health System | 0 | 1 | 14 | 3 | 0 | 18 |
| Juno Genomics, Hangzhou Juno Genomics, Inc | 0 | 2 | 0 | 0 | 0 | 2 |
| Institute of Human Genetics, Heidelberg University | 0 | 1 | 0 | 0 | 0 | 1 |
| Mayo Clinic Laboratories, Mayo Clinic | 0 | 0 | 1 | 0 | 0 | 1 |
| Otogenetics | 0 | 1 | 0 | 0 | 0 | 1 |