Total submissions: 5
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Color Diagnostics, |
RCV000581378 | SCV000687470 | likely benign | Hereditary cancer-predisposing syndrome | 2016-11-22 | criteria provided, single submitter | clinical testing | |
Women's Health and Genetics/Laboratory Corporation of America, |
RCV000590240 | SCV000694260 | uncertain significance | not provided | 2016-03-18 | criteria provided, single submitter | clinical testing | |
Gene |
RCV000590240 | SCV001945470 | benign | not provided | 2015-03-03 | criteria provided, single submitter | clinical testing | |
Invitae | RCV002060596 | SCV002416534 | likely benign | Ataxia-telangiectasia syndrome | 2024-01-24 | criteria provided, single submitter | clinical testing | |
KCCC/NGS Laboratory, |
RCV003316756 | SCV004016719 | likely benign | Familial cancer of breast | 2023-07-07 | criteria provided, single submitter | clinical testing |