ClinVar Miner

List of variants in gene MYH7 reported as likely pathogenic by Center for Human Genetics, University of Leuven

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Total variants: 6
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HGVS dbSNP gnomAD frequency
NM_000257.4(MYH7):c.1324C>T (p.Arg442Cys) rs148808089 0.00001
NM_000257.4(MYH7):c.1325G>T (p.Arg442Leu) rs730880870
NM_000257.4(MYH7):c.2207T>C (p.Ile736Thr) rs727503261
NM_000257.4(MYH7):c.2707G>A (p.Glu903Lys) rs730880756
NM_000257.4(MYH7):c.952A>C (p.Thr318Pro) rs1566536436
NM_000257.4(MYH7):c.959T>A (p.Val320Glu) rs1566536418

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