Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Gene |
RCV000439839 | SCV000529973 | likely benign | not provided | 2018-09-06 | criteria provided, single submitter | clinical testing | |
Invitae | RCV000791920 | SCV000931189 | benign | Hereditary sensory neuropathy-deafness-dementia syndrome | 2023-08-10 | criteria provided, single submitter | clinical testing | |
Ce |
RCV000439839 | SCV004146639 | likely benign | not provided | 2022-09-01 | criteria provided, single submitter | clinical testing | DNMT1: BP4, BP7 |