ClinVar Miner

List of variants in gene MYH7 reported as uncertain significance for Primary dilated cardiomyopathy

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Total variants: 22
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HGVS dbSNP gnomAD frequency
NM_000257.4(MYH7):c.2890G>C (p.Val964Leu) rs45496496 0.00050
NM_000257.4(MYH7):c.161G>A (p.Arg54Gln) rs397516117 0.00003
NM_000257.4(MYH7):c.1856C>T (p.Thr619Ile) rs541143322 0.00002
NM_000257.4(MYH7):c.1700G>A (p.Arg567His) rs377491278 0.00001
NM_000257.4(MYH7):c.3866G>A (p.Arg1289Gln) rs1287612987 0.00001
NM_000257.4(MYH7):c.5530G>A (p.Glu1844Lys) rs730880821 0.00001
NM_000257.4(MYH7):c.5588G>A (p.Arg1863Gln) rs45520836 0.00001
NM_000257.4(MYH7):c.821T>C (p.Ile274Thr) rs773456019 0.00001
NM_000257.4(MYH7):c.1128C>A (p.Asp376Glu) rs2231126
NM_000257.4(MYH7):c.1565A>T (p.Asp522Val) rs1595086146
NM_000257.4(MYH7):c.1997A>G (p.His666Arg) rs769919688
NM_000257.4(MYH7):c.3020T>C (p.Leu1007Pro) rs730880763
NM_000257.4(MYH7):c.323G>A (p.Arg108His) rs730880832
NM_000257.4(MYH7):c.3634C>T (p.Arg1212Trp) rs1555337102
NM_000257.4(MYH7):c.3929A>C (p.Gln1310Pro) rs869025481
NM_000257.4(MYH7):c.475G>C (p.Asp159His) rs730880155
NM_000257.4(MYH7):c.5395G>A (p.Glu1799Lys) rs730880816
NM_000257.4(MYH7):c.5413C>A (p.Leu1805Ile) rs1892134324
NM_000257.4(MYH7):c.5494C>T (p.Arg1832Cys) rs201865159
NM_000257.4(MYH7):c.5726G>C (p.Arg1909Pro) rs397516253
NM_000257.4(MYH7):c.5767A>G (p.Lys1923Glu) rs1595070373
NM_000257.4(MYH7):c.5769del (p.Ser1924fs) rs1892066954

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