Total submissions: 7
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Prevention |
RCV000243896 | SCV000306859 | benign | not specified | criteria provided, single submitter | clinical testing | ||
Gene |
RCV001668463 | SCV001884419 | benign | not provided | 2018-06-24 | criteria provided, single submitter | clinical testing | |
Genome- |
RCV001775711 | SCV002014400 | benign | Peripheral neuropathy-myopathy-hoarseness-hearing loss syndrome | 2021-09-05 | criteria provided, single submitter | clinical testing | |
Genome- |
RCV001775710 | SCV002014401 | benign | Autosomal dominant nonsyndromic hearing loss 4A | 2021-09-05 | criteria provided, single submitter | clinical testing | |
Invitae | RCV001668463 | SCV002410208 | benign | not provided | 2024-01-31 | criteria provided, single submitter | clinical testing | |
Clinical Genetics, |
RCV000243896 | SCV001918835 | benign | not specified | no assertion criteria provided | clinical testing | ||
Diagnostic Laboratory, |
RCV000243896 | SCV001963283 | benign | not specified | no assertion criteria provided | clinical testing |