Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV000534996 | SCV000636492 | pathogenic | Bardet-Biedl syndrome | 2018-08-16 | criteria provided, single submitter | clinical testing | A gross deletion of the genomic region encompassing the full coding sequence of the TRIM32 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. This variant has been reported in the literature in individuals affected with limb girdle muscular dystrophy (PMID: 25351777, 23541687). Loss-of-function variants in TRIM32 are known to be pathogenic (PMID: 23541687). For these reasons, this variant has been classified as Pathogenic. |