ClinVar Miner

List of variants in gene combination MHRT, MYH7 reported as likely benign for Cardiomyopathy

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Total variants: 13
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HGVS dbSNP
NM_000257.4(MYH7):c.4293C>T (p.Asp1431=) rs45560242
NM_000257.4(MYH7):c.4377G>T (p.Lys1459Asn) rs201307101
NM_000257.4(MYH7):c.4520-3C>T rs549509054
NM_000257.4(MYH7):c.4605C>T (p.Ala1535=) rs746261895
NM_000257.4(MYH7):c.4618C>T (p.Leu1540=) rs368734580
NM_000257.4(MYH7):c.4644+3G>A rs397516226
NM_000257.4(MYH7):c.4689G>A (p.Leu1563=) rs770477774
NM_000257.4(MYH7):c.4725G>A (p.Lys1575=) rs45476496
NM_000257.4(MYH7):c.4834C>T (p.Leu1612=) rs397516229
NM_000257.4(MYH7):c.4893C>T (p.His1631=) rs369164804
NM_000257.4(MYH7):c.4908C>T (p.Ala1636=) rs150241539
NM_000257.4(MYH7):c.4941G>A (p.Gln1647=) rs749154313
NM_000257.4(MYH7):c.5061G>A (p.Glu1687=) rs1410160839

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