"Revvity Omics, Revvity"[submitter] AND "RBM20"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 937622	NM_001134363.3(RBM20):c.83G>A (p.Gly28Asp)	RBM20 (G28D)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1DD +1 more	GConflicting classifications of pathogenicity
Select item 2435382	NM_001134363.3(RBM20):c.458C>T (p.Pro153Leu)	RBM20 (P153L)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1DD	GUncertain significance
Select item 2435383	NM_001134363.3(RBM20):c.556C>T (p.Leu186Phe)	RBM20 (L186F)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1DD	GUncertain significance
Select item 268	NM_001134363.3(RBM20):c.1913C>T (p.Pro638Leu)	RBM20 (P638L)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +5 more	GPathogenic
Select item 180045	NM_001134363.3(RBM20):c.1958C>T (p.Thr653Ile)	RBM20 (T653I)	Single nucleotide variant (missense variant)	not specified +3 more	GConflicting classifications of pathogenicity
Select item 43991	NM_001134363.3(RBM20):c.2551G>A (p.Ala851Thr)	RBM20 (A851T)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1DD +3 more	GUncertain significance
Select item 238553	NM_001134363.3(RBM20):c.3268A>T (p.Ile1090Phe)	RBM20 (I1090F)	Single nucleotide variant (missense variant)	not provided +2 more	GConflicting classifications of pathogenicity

ClinVar