ClinVar Miner

List of variants in gene combination MHRT, MYH7 reported as likely benign for not provided

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Total variants: 9
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HGVS dbSNP
NM_000257.4(MYH7):c.4353+10G>A rs202205780
NM_000257.4(MYH7):c.4354-61A>T
NM_000257.4(MYH7):c.4452C>T (p.Leu1484=) rs61737803
NM_000257.4(MYH7):c.4645-273T>C
NM_000257.4(MYH7):c.4806C>T (p.Asp1602=) rs142034311
NM_000257.4(MYH7):c.4954-41G>A
NM_000257.4(MYH7):c.5062T>C (p.Leu1688=) rs768580382
NM_000257.4(MYH7):c.5067T>G (p.Arg1689=)
NM_000257.4(MYH7):c.5079G>A (p.Glu1693=)

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