ClinVar Miner

List of variants in gene combination MHRT, MYH7 reported as likely benign by GeneDx

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Total variants: 27
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HGVS dbSNP
NM_000257.4(MYH7):c.4275C>A (p.Ile1425=) rs57680382
NM_000257.4(MYH7):c.4275C>T (p.Ile1425=) rs57680382
NM_000257.4(MYH7):c.4293C>T (p.Asp1431=) rs45560242
NM_000257.4(MYH7):c.4353+6C>T rs765398896
NM_000257.4(MYH7):c.4354-61A>T
NM_000257.4(MYH7):c.4371G>A (p.Lys1457=) rs1555336697
NM_000257.4(MYH7):c.4377G>T (p.Lys1459Asn) rs201307101
NM_000257.4(MYH7):c.4395G>T (p.Ser1465=) rs397516213
NM_000257.4(MYH7):c.4410G>A (p.Ser1470=) rs578166720
NM_000257.4(MYH7):c.4513C>T (p.Leu1505=) rs139928934
NM_000257.4(MYH7):c.4644+3G>A rs397516226
NM_000257.4(MYH7):c.4644+7G>C rs1555336564
NM_000257.4(MYH7):c.4645-16C>T rs778453839
NM_000257.4(MYH7):c.4645-17C>T rs1555336497
NM_000257.4(MYH7):c.4645-273T>C
NM_000257.4(MYH7):c.4725G>A (p.Lys1575=) rs45476496
NM_000257.4(MYH7):c.4800C>T (p.Ser1600=) rs1057521761
NM_000257.4(MYH7):c.4869T>C (p.Asn1623=) rs1448315071
NM_000257.4(MYH7):c.4893C>T (p.His1631=) rs369164804
NM_000257.4(MYH7):c.4941G>A (p.Gln1647=) rs749154313
NM_000257.4(MYH7):c.4953+13A>T rs373509029
NM_000257.4(MYH7):c.4954-14C>T rs727505070
NM_000257.4(MYH7):c.4954-41G>A
NM_000257.4(MYH7):c.5067T>G (p.Arg1689=)
NM_000257.4(MYH7):c.5070C>G (p.Ala1690=) rs764844610
NM_000257.4(MYH7):c.5079G>A (p.Glu1693=)
NM_000257.4(MYH7):c.5158-15C>T rs369453980

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