"Fulgent Genetics, Fulgent Genetics"[submitter] AND "CDH2"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 789103	NM_001792.5(CDH2):c.885C>T (p.Asp295=)	CDH2	Single nucleotide variant (synonymous variant)	Arrhythmogenic right ventricular dysplasia, familial, 14 +3 more	GBenign/Likely benign
Select item 789104	NM_001792.5(CDH2):c.702+6A>T	CDH2	Single nucleotide variant (intron variant)	Arrhythmogenic right ventricular dysplasia, familial, 14 +2 more	GBenign/Likely benign