List of variants in gene combination ABCC9, KCNJ8 reported as benign for Cardiomyopathy

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_020297.4(ABCC9):c.3768T>C (p.Leu1256=)	rs150303433	0.00209
NM_020297.4(ABCC9):c.4450-5del	rs4148680
NM_020297.4(ABCC9):c.4450-5dup	rs4148680

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