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Achromatopsia
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Alagille syndrome
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Deafness_IsolatedAndComplex
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Ectodermal Dysplasia
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IBMDx study
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Incidentalome_PREGEN_DRAFT
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Kabuki syndrome
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Kidneyome_SuperPanel
Leukodystrophy
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Lipodystrophy_Lipoatrophy
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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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Pierre Robin Sequence
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Prepair 1000+
Prepair 500+
Primary nodular adrenocortical disease
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Progressive Myoclonic Epilepsy
Progressive Neurological Conditions
Prostate Cancer
Proteinuria
Pseudohypoparathyroidism and Albright Hereditary Osteodystrophy
Pulmonary Arterial Hypertension
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Renal Cystic Disease_SuperPanel
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Retinal Disorders Superpanel
Retinitis pigmentosa
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Short QT syndrome
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Thyroid Cancer
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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
0.395
Gene or Genomic Entity Name
KARS1
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07 Jun 2026
Leukodystrophy v1.0
KARS1
Gene symbol changed from KARS to KARS1 during gene set migration (ENSG00000065427 -> ENSG00000065427)