Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV000707898 | SCV000837008 | pathogenic | Majeed syndrome | 2019-09-24 | criteria provided, single submitter | clinical testing | A gross deletion of the genomic region encompassing the full coding sequence of the LPIN2 gene has been identified. The boundaries of this event are unknown as the deletion extends beyond the assayed region for this gene and therefore may encompass additional genes. Gross deletions have not been reported in the literature in individuals with LPIN2-related disease Loss-of-function variants in LPIN2 are known to be pathogenic (PMID: 15994876, 23087183). For these reasons, this variant has been classified as Pathogenic. |