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Achromatopsia
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Alagille syndrome
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Incidentalome_PREGEN_DRAFT
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Liverome Superpanel
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Myopathy Superpanel
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Pierre Robin Sequence
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Prepair 1000+
Prepair 500+
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Tubulinopathies
Usher Syndrome
Vascular Malformations_Germline
Vascular Malformations_Somatic
Vascular Malformations SuperPanel
Vitamin metabolism disorders
Vitreoretinopathy
Wilms Tumour
Version
Panel Version
1.0
0.272
Gene or Genomic Entity Name
CNBP_DM2_CCTG
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07 Jun 2026
Repeat Disorders v1.0
CNBP_DM2_CCTG
STR CNBP_DM2_CCTG: gene migrated from ENSG00000169714 to ENSG00000169714 (gene set migration)
24 Apr 2025
Repeat Disorders v0.176
CNBP_DM2_CCTG
Bryony Thompson DM2 was changed to CNBP_DM2_CCTG