List of variants in gene MYH6 reported as uncertain significance for Primary dilated cardiomyopathy

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 14

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HGVS	dbSNP	gnomAD frequency
NM_002471.4(MYH6):c.2614C>T (p.Arg872Cys)	rs201193346	0.00022
NM_002471.4(MYH6):c.4505G>A (p.Arg1502Gln)	rs199936506	0.00022
NM_002471.4(MYH6):c.4328C>A (p.Ala1443Asp)	rs727503234	0.00019
NM_002471.4(MYH6):c.824T>A (p.Ile275Asn)	rs201327273	0.00019
NM_002471.4(MYH6):c.1132G>A (p.Gly378Ser)	rs148962966	0.00014
NM_002471.4(MYH6):c.1171C>A (p.Leu391Met)	rs869025472	0.00006
NM_002471.4(MYH6):c.4216G>A (p.Val1406Met)	rs201566738	0.00006
NM_002471.4(MYH6):c.3583C>T (p.Arg1195Cys)	rs769756450	0.00003
NM_002471.4(MYH6):c.3133A>G (p.Lys1045Glu)	rs869025474	0.00001
NM_002471.4(MYH6):c.4471G>A (p.Glu1491Lys)	rs1314169075	0.00001
NM_002471.4(MYH6):c.1334A>G (p.Asn445Ser)
NM_002471.4(MYH6):c.2538G>C (p.Glu846Asp)	rs730880150
NM_002471.4(MYH6):c.4231G>A (p.Ala1411Thr)
NM_002471.4(MYH6):c.5476_5477delinsAA (p.Gly1826Asn)	rs878854502

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