C2750995[trait identifier] AND "Center for Genomics, Ann and Robert H. - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 44024	NM_001134363.3(RBM20):c.530C>T (p.Thr177Ile)	RBM20 (T177I)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +4 more	GConflicting classifications of pathogenicity
Select item 1051356	NM_001134363.3(RBM20):c.676G>A (p.Ala226Thr)	RBM20 (A226T)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 229182	NM_001134363.3(RBM20):c.1024C>A (p.Pro342Thr)	RBM20 (P342T)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +3 more	GConflicting classifications of pathogenicity
Select item 962316	NM_001134363.3(RBM20):c.1643A>G (p.Tyr548Cys)	RBM20 (Y548C)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1DD	GUncertain significance
Select item 43978	NM_001134363.3(RBM20):c.1880+4_1880+6dup	RBM20	Duplication (intron variant)	Cardiovascular phenotype +5 more	GConflicting classifications of pathogenicity
Select item 1439812	NM_001134363.3(RBM20):c.2410G>A (p.Glu804Lys)	RBM20 (E804K)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1DD	GConflicting classifications of pathogenicity

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