Total submissions: 6
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Preventiongenetics, |
RCV000251165 | SCV000306677 | benign | not specified | criteria provided, single submitter | clinical testing | ||
Invitae | RCV001510736 | SCV001717844 | benign | Frontotemporal dementia | 2024-01-19 | criteria provided, single submitter | clinical testing | |
Gene |
RCV000084503 | SCV001833087 | benign | not provided | 2018-08-11 | criteria provided, single submitter | clinical testing | This variant is associated with the following publications: (PMID: 23222517) |
VIB Department of Molecular Genetics, |
RCV000084503 | SCV000116639 | not provided | not provided | no assertion provided | not provided | ||
Genome Diagnostics Laboratory, |
RCV000251165 | SCV001807300 | benign | not specified | no assertion criteria provided | clinical testing | ||
Clinical Genetics, |
RCV000251165 | SCV001923233 | benign | not specified | no assertion criteria provided | clinical testing |