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Achromatopsia
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Genomic newborn screening: BabyScreen+
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IBMDx study
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Incidentalome_PREGEN_DRAFT
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Kidneyome_SuperPanel
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Liverome Superpanel
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Mackenzie's Mission_Reproductive Carrier Screening
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Myopathy Superpanel
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Pharmacogenomics_Paediatric
Photosensitivity Syndromes
Pierre Robin Sequence
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Prepair 1000+
Prepair 500+
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Prostate Cancer
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Renal Cystic Disease_SuperPanel
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Retinal Disorders Superpanel
Retinitis pigmentosa
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Severe Combined Immunodeficiency
Severe early-onset obesity
Short QT syndrome
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Speech apraxia
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Stickler Syndrome
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Susceptibility to Viral Infections
Syndromic Retinopathy
Thyroid Cancer
Transplant Co-Morbidity
Tuberous Sclerosis_Focal Cortical Dysplasia_Hemimegalencephaly
Tubulinopathies
Usher Syndrome
Vascular Malformations_Germline
Vascular Malformations_Somatic
Vascular Malformations SuperPanel
Vitamin metabolism disorders
Vitreoretinopathy
Wilms Tumour
Version
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1.0
0.280
Gene or Genomic Entity Name
DNAAF19
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07 Jun 2026
Additional findings_Paediatric v1.0
DNAAF19
Gene symbol changed from CCDC103 to DNAAF19 during gene set migration (ENSG00000167131 -> ENSG00000167131)