C1836050[trait identifier] AND "Molecular Genetics, Royal Melbourne Ho - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 432231	NM_001458.5(FLNC):c.970-4A>G	FLNC	Single nucleotide variant (intron variant)	Hypertrophic cardiomyopathy 26 +8 more	GConflicting classifications of pathogenicity
Select item 960797	NM_001458.5(FLNC):c.1131G>C (p.Lys377Asn)	FLNC (K377N)	Single nucleotide variant (missense variant)	Myofibrillar myopathy 5 +3 more	GUncertain significance
Select item 1479172	NM_001458.5(FLNC):c.1468C>T (p.Arg490Cys)	FLNC (R490C)	Single nucleotide variant (missense variant)	Primary dilated cardiomyopathy +6 more	GUncertain significance
Select item 664906	NM_001458.5(FLNC):c.1885C>T (p.Arg629Trp)	FLNC (R629W)	Single nucleotide variant (missense variant)	Distal myopathy with posterior leg and anterior hand involvement +5 more	GConflicting classifications of pathogenicity
Select item 579589	NM_001458.5(FLNC):c.3937C>T (p.Arg1313Ter)	FLNC (R1313*)	Single nucleotide variant (nonsense)	Primary dilated cardiomyopathy +6 more	GPathogenic/Likely pathogenic
Select item 539333	NM_001458.5(FLNC):c.7226G>A (p.Arg2409His)	FLNC, FLNC-AS1 (R2409H +1 more)	Single nucleotide variant (missense variant)	Myofibrillar myopathy 5 +5 more	GConflicting classifications of pathogenicity

ClinVar