C2751083[trait identifier] AND "Center for Genomics, Ann and Robert H. - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 412788	NM_005477.3(HCN4):c.1243G>A (p.Val415Met)	HCN4 (V415M)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +5 more	GConflicting classifications of pathogenicity
Select item 180370	NM_005477.3(HCN4):c.458A>G (p.Glu153Gly)	HCN4 (E153G)	Single nucleotide variant (missense variant)	Primary dilated cardiomyopathy +7 more	GConflicting classifications of pathogenicity