Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Institute Of Human Genetics Munich, |
RCV000172913 | SCV000680176 | pathogenic | Hypomagnesemia, seizures, and intellectual disability 1 | 2017-10-12 | criteria provided, single submitter | clinical testing | |
OMIM | RCV000172913 | SCV000223897 | pathogenic | Hypomagnesemia, seizures, and intellectual disability 1 | 2014-04-01 | no assertion criteria provided | literature only |