List of variants reported as uncertain significance for Congestive heart failure

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_014000.3(VCL):c.1490T>C (p.Ile497Thr)	rs572757800	0.00008
NM_002471.4(MYH6):c.3988G>A (p.Ala1330Thr)	rs757840030	0.00007
NM_001035.3(RYR2):c.10640C>T (p.Thr3547Met)	rs552050895	0.00004
NM_016203.4(PRKAG2):c.431C>T (p.Pro144Leu)	rs150140412	0.00002

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