ClinVar Miner

List of variants in gene MYH7 reported as uncertain significance by Mayo Clinic Laboratories, Mayo Clinic

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Gene type:
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Total variants: 16
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HGVS dbSNP gnomAD frequency
NM_000257.4(MYH7):c.3726+6C>T rs377745688 0.00013
NM_000257.4(MYH7):c.5786C>T (p.Thr1929Met) rs730880918 0.00010
NM_000257.4(MYH7):c.2206A>G (p.Ile736Val) rs397516138 0.00004
NM_000257.4(MYH7):c.1633G>A (p.Asp545Asn) rs564101364 0.00001
NM_000257.4(MYH7):c.1756G>A (p.Val586Met) rs754465530 0.00001
NM_000257.4(MYH7):c.1948C>A (p.Leu650Met) rs1892728965 0.00001
NM_000257.4(MYH7):c.328G>A (p.Gly110Ser) rs763893822 0.00001
NM_000257.4(MYH7):c.3778C>T (p.Arg1260Trp) rs755386220 0.00001
NM_000257.4(MYH7):c.4145G>A (p.Arg1382Gln) rs727504325 0.00001
NM_000257.4(MYH7):c.1187T>G (p.Leu396Arg) rs1060501447
NM_000257.4(MYH7):c.2810C>A (p.Thr937Asn)
NM_000257.4(MYH7):c.2858A>T (p.Asp953Val) rs730880901
NM_000257.4(MYH7):c.2863G>A (p.Asp955Asn) rs886039204
NM_000257.4(MYH7):c.323G>A (p.Arg108His) rs730880832
NM_000257.4(MYH7):c.3592G>A (p.Asp1198Asn) rs730880778
NM_000257.4(MYH7):c.5767A>G (p.Lys1923Glu) rs1595070373

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