ClinVar Miner

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

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Gene type:
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Total variants: 7
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HGVS dbSNP
NM_000257.4(MYH7):c.4341G>A (p.Arg1447=) rs778233579
NM_000257.4(MYH7):c.4347C>T (p.Phe1449=) rs182311329
NM_000257.4(MYH7):c.4513C>T (p.Leu1505=) rs139928934
NM_000257.4(MYH7):c.4671G>A (p.Lys1557=) rs200601164
NM_000257.4(MYH7):c.4965T>C (p.Ile1655=) rs886039010
NM_000257.4(MYH7):c.4980A>G (p.Ala1660=) rs112943492
NM_000257.4(MYH7):c.5139G>A (p.Val1713=) rs369562442

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