"Mayo Clinic Laboratories, Mayo Clinic"[submitter] AND "ANKRD1"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 201668	NM_014391.3(ANKRD1):c.881A>G (p.His294Arg)	ANKRD1 (H294R)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +3 more	GUncertain significance
Select item 162750	NM_014391.3(ANKRD1):c.234A>T (p.Arg78Ser)	ANKRD1 (R78S)	Single nucleotide variant (missense variant)	not provided +3 more	GUncertain significance
Select item 201670	NM_014391.3(ANKRD1):c.222dup (p.Leu75fs)	ANKRD1 (L75fs)	Duplication	ANKRD1-related dilated cardiomyopathy +4 more	GUncertain significance

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