ClinVar Miner

List of variants in gene combination MHRT, MYH7 reported as uncertain significance by Biesecker Lab/Clinical Genomics Section,National Institutes of Health

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Gene type:
ClinVar version:
Total variants: 3
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HGVS dbSNP
NM_000257.4(MYH7):c.4321G>T (p.Ala1441Ser) rs745414245
NM_000257.4(MYH7):c.4707G>T (p.Lys1569Asn) rs199557822
NM_000257.4(MYH7):c.4816C>T (p.Arg1606Cys) rs200530211

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