Related gene-specific medical variations for Gene (Select 808) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1179377	NM_005184.3(CALM3):c.-177G>A	CALM3, LOC130064760	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1167461	NC_000019.10:g.46601278T>A	CALM3, LOC130064760	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 812677	A103V	CALM3	Variation	Ventricular tachycardia, catecholaminergic polymorphic 6	GPathogenic

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