List of variants reported as uncertain significance for cardiomyopathy by Center for Human Genetics, Inc, Center for Human Genetics, Inc

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Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_005343.4(HRAS):c.81T>C (p.His27=)	rs12628	0.34645
NM_152594.3(SPRED1):c.926T>C (p.Val309Ala)	rs114636635	0.00204
NM_002880.4(RAF1):c.119G>A (p.Arg40His)	rs192632236	0.00016
NM_004333.6(BRAF):c.1382A>G (p.Gln461Arg)	rs1554399925

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