"Centre for Mendelian Genomics, University Medical Centre Ljubljana"[s - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 167533	NM_016203.4(PRKAG2):c.1304A>G (p.Asn435Ser)	PRKAG2 (N435S +4 more)	Single nucleotide variant (missense variant)	Cardiomyopathy +5 more	GConflicting classifications of pathogenicity
Select item 6846	NM_016203.4(PRKAG2):c.905G>A (p.Arg302Gln)	PRKAG2 (R302Q +4 more)	Single nucleotide variant (missense variant)	Familial Hypertrophic Cardiomyopathy with Wolff-Parkinson-White Syndrome +8 more	GPathogenic
Select item 45733	NM_016203.4(PRKAG2):c.698C>G (p.Ala233Gly)	LOC129999660, PRKAG2 (A233G +2 more)	Single nucleotide variant (missense variant +1 more)	not specified +8 more	GConflicting classifications of pathogenicity
Select item 374128	NM_016203.4(PRKAG2):c.590C>G (p.Pro197Arg)	PRKAG2 (P197R +2 more)	Single nucleotide variant (missense variant)	Wolff-Parkinson-White pattern +9 more	GUncertain significance
Select item 45717	NM_016203.4(PRKAG2):c.425C>T (p.Thr142Ile)	PRKAG2 (T142I +1 more)	Single nucleotide variant (missense variant)	Hypertrophic cardiomyopathy 6 +7 more	GConflicting classifications of pathogenicity
Select item 931949	NM_016203.4(PRKAG2):c.413C>G (p.Ser138Cys)	PRKAG2 (S138C +1 more)	Single nucleotide variant (missense variant)	Wolff-Parkinson-White pattern	GUncertain significance

ClinVar