Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV001032807 | SCV001196114 | pathogenic | Duchenne muscular dystrophy | 2019-05-09 | criteria provided, single submitter | clinical testing | This variant results in a copy number gain of the genomic region encompassing exon 52 of the DMD gene. While the exact position of this variant cannot be determined from this data, sub-genic copy number gains are generally in tandem (PMID: 25640679) and may result in an absent or disrupted protein product. This variant has been observed in several individuals affected with Duchenne muscular dystrophy (PMID: 20381484, 23818053, 28116794, 28610567). Loss-of-function variants in DMD are known to be pathogenic (PMID: 16770791, 25007885). For these reasons, this variant has been classified as Pathogenic. |