ClinVar Miner

Submissions for variant NC_000023.11:g.(?_13735066)_(13769113_?)del

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001031300 SCV001194606 pathogenic Familial aplasia of the vermis; Orofaciodigital syndrome I 2019-01-11 criteria provided, single submitter clinical testing A gross deletion of the genomic region encompassing the full coding sequence of the OFD1 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. A similar gross deletion of OFD1 has been reported in individuals affected with Oral-facial-digital syndrome (PMID: 23033313) or Joubert syndrome (PMID:24476948). In one of the individuals affected with Oral-facial-digital syndrome the variant was reported as de novo (PMID: 23033313). Loss-of-function variants in OFD1 are known to be pathogenic (PMID: 16783569, 18546297, 27081566). For these reasons, this variant has been classified as Pathogenic.

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