CN315764[trait identifier] AND "OMIM"[submitter] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 8293	NM_033337.3(CAV3):c.233C>T (p.Thr78Met)	CAV3, OXTR (T78M)	Single nucleotide variant (missense variant)	CAV3-related condition +8 more	GConflicting classifications of pathogenicity
Select item 14443	NM_000238.4(KCNH2):c.2738C>T (p.Ala913Val)	KCNH2 (A573V +2 more)	Single nucleotide variant (missense variant)	Cardiac arrhythmia +4 more	GConflicting classifications of pathogenicity