"CALM3-related disorder"[Disease/phenotype] AND "PreventionGenetics, p - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1166599	NM_005184.4(CALM3):c.249G>A (p.Glu83=)	CALM3	Single nucleotide variant (synonymous variant)	Long QT syndrome 1 +2 more	GBenign/Likely benign
Select item 458196	NM_005184.4(CALM3):c.309C>T (p.Ala103=)	CALM3	Single nucleotide variant (synonymous variant)	CALM3-related disorder +3 more	GLikely benign