Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Laboratory of Human Genetics, |
RCV000785977 | SCV000924343 | pathogenic | Syndromic X-linked intellectual disability Claes-Jensen type | 2019-06-19 | criteria provided, single submitter | research | |
Mendelics | RCV000785977 | SCV001141872 | likely pathogenic | Syndromic X-linked intellectual disability Claes-Jensen type | 2019-05-28 | criteria provided, single submitter | clinical testing | |
OMIM | RCV000785977 | SCV002549036 | pathogenic | Syndromic X-linked intellectual disability Claes-Jensen type | 2022-07-15 | no assertion criteria provided | literature only |