Clinical and research tests for Tinus candolleana - Genetic Testing Registry (GTR)

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Select all conditions on this page	Gene symbol	Associated conditionsHelp Conditions and phenotypes associated with each gene as reported by OMIM, GeneReviews and Gene
Select item 775	CACNA1C	Brugada syndrome 3 Long qt syndrome 8 Neurodevelopmental disorder with hypotonia, language delay, and skeletal defects with or without seizures Timothy syndrome
Select item 783	CACNB2	Brugada syndrome 4
Select item 57647	DHX37	46,XY sex reversal 11 Neurodevelopmental disorder with brain anomalies and with or without vertebral or cardiac anomalies
Select item 2783	GNB2	Neurodevelopmental disorder with hypotonia and dysmorphic facies Sick sinus syndrome 4
Select item 10681	GNB5	Gnb5-related intellectual disability-cardiac arrhythmia syndrome Language delay and attention deficit-hyperactivity disorder/cognitive impairment with or without cardiac arrhythmia
Select item 23171	GPD1L	Brugada syndrome 2
Select item 10021	HCN4	Brugada syndrome 8 Epilepsy, idiopathic generalized, susceptibility to, 18 Sick sinus syndrome 2, autosomal dominant
Select item 3621	ING1	Squamous cell carcinoma of the head and neck
Select item 3664	IRF6	Autosomal dominant popliteal pterygium syndrome Orofacial cleft 6, susceptibility to Van der Woude syndrome 1
Select item 3752	KCND3	Brugada syndrome 9 Hereditary ataxia Spinocerebellar ataxia type 19/22
Select item 10008	KCNE3	Brugada syndrome 6
Select item 8085	KMT2D	Branchial arch abnormalities, choanal atresia, athelia, hearing loss, and hypothyroidism syndrome Kabuki syndrome 1
Select item 4624	MYH6	Atrial septal defect 3 Dilated cardiomyopathy 1EE Hypertrophic cardiomyopathy 1 Hypertrophic cardiomyopathy 14 Primary dilated cardiomyopathy Sick sinus syndrome 3, susceptibility to
Select item 283446	MYO1H	Central hypoventilation syndrome, congenital, 2, and autonomic dysfunction
Select item 8929	PHOX2B	Central hypoventilation syndrome, congenital, 1, with or without Hirschsprung disease Neuroblastoma, susceptibility to, 2
Select item 4659	PPP1R12A	Genitourinary and/or brain malformation syndrome
Select item 860	RUNX2	Cleidocranial dysostosis Metaphyseal dysplasia-maxillary hypoplasia-brachydacty syndrome
Select item 6324	SCN1B	Atrial fibrillation, familial, 13 Brugada syndrome 5 Developmental and epileptic encephalopathy, 52 Generalized epilepsy with febrile seizures plus, type 1
Select item 55800	SCN3B	Brugada syndrome 7
Select item 6331	SCN5A	Atrial fibrillation, familial, 10 Brugada syndrome 1 Dilated cardiomyopathy 1E Long QT syndrome Long QT syndrome 3 Progressive familial heart block, type 1A Sick sinus syndrome 1 SUDDEN INFANT DEATH SYNDROME Ventricular fibrillation, paroxysmal familial, type 1

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