Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV001387105 | SCV001587620 | pathogenic | Autosomal recessive distal spinal muscular atrophy 1; Charcot-Marie-Tooth disease axonal type 2S | 2020-08-11 | criteria provided, single submitter | clinical testing | A gross deletion of the genomic region encompassing the full coding sequence of the IGHMBP2 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 not been reported in the literature in individuals with IGHMBP2-related conditions. Loss-of-function variants in IGHMBP2 are known to be pathogenic (PMID: 14681881). For these reasons, this variant has been classified as Pathogenic. |