ClinVar Miner

List of variants in gene combination MHRT, MYH7 reported as uncertain significance by Stanford Center for Inherited Cardiovascular Disease,Stanford University

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Gene type:
ClinVar version:
Total variants: 6
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NM_000257.4(MYH7):c.4363G>A (p.Glu1455Lys) rs876661373
NM_000257.4(MYH7):c.4402G>A (p.Glu1468Lys) rs876657884
NM_000257.4(MYH7):c.4519+1G>C rs876661374
NM_000257.4(MYH7):c.4588C>T (p.Arg1530Ter) rs397516225
NM_000257.4(MYH7):c.4679G>A (p.Arg1560Gln) rs730880806
NM_000257.4(MYH7):c.4817G>A (p.Arg1606His) rs373514686

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