ClinVar Miner

List of variants in gene MYH6 reported as uncertain significance by GeneDx

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Total variants: 42
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HGVS dbSNP
NM_002471.3(MYH6):c.1177T>G (p.Ser393Ala) rs199877580
NM_002471.3(MYH6):c.1373T>C (p.Ile458Thr) rs774807696
NM_002471.3(MYH6):c.1521T>G (p.Ile507Met) rs142410102
NM_002471.3(MYH6):c.1628A>G (p.Lys543Arg) rs367663906
NM_002471.3(MYH6):c.1753G>A (p.Gly585Ser) rs150415679
NM_002471.3(MYH6):c.1784T>A (p.Leu595Gln) rs751418733
NM_002471.3(MYH6):c.1960C>T (p.Arg654Trp) rs369938365
NM_002471.3(MYH6):c.2114G>A (p.Arg705His) rs754654593
NM_002471.3(MYH6):c.2141G>A (p.Arg714His) rs776602843
NM_002471.3(MYH6):c.2141G>T (p.Arg714Leu) rs776602843
NM_002471.3(MYH6):c.2575G>A (p.Gly859Arg) rs369274077
NM_002471.3(MYH6):c.2578C>A (p.Arg860Ser) rs1025146248
NM_002471.3(MYH6):c.2597A>G (p.Glu866Gly) rs886039171
NM_002471.3(MYH6):c.2611C>T (p.Arg871Cys) rs376682837
NM_002471.3(MYH6):c.3155G>A (p.Arg1052Gln) rs750020902
NM_002471.3(MYH6):c.3230A>T (p.Gln1077Leu) rs377716628
NM_002471.3(MYH6):c.3299A>T (p.Gln1100Leu) rs775652096
NM_002471.3(MYH6):c.3346C>A (p.Arg1116Ser) rs372446459
NM_002471.3(MYH6):c.3347G>A (p.Arg1116His) rs369247906
NM_002471.3(MYH6):c.3383G>A (p.Arg1128His) rs376002621
NM_002471.3(MYH6):c.3469G>A (p.Gly1157Arg) rs755974106
NM_002471.3(MYH6):c.3481G>A (p.Val1161Met) rs762230455
NM_002471.3(MYH6):c.3584G>A (p.Arg1195His) rs747891865
NM_002471.3(MYH6):c.3758C>T (p.Thr1253Met) rs201051663
NM_002471.3(MYH6):c.3809G>A (p.Arg1270His) rs767603407
NM_002471.3(MYH6):c.3835C>T (p.Arg1279Ter) rs751426149
NM_002471.3(MYH6):c.4016G>A (p.Arg1339Gln) rs766238876
NM_002471.3(MYH6):c.4394C>T (p.Ser1465Leu) rs766327056
NM_002471.3(MYH6):c.4651-3C>A rs572175190
NM_002471.3(MYH6):c.4665C>A (p.His1555Gln) rs373888186
NM_002471.3(MYH6):c.4727G>A (p.Arg1576Gln) rs771898553
NM_002471.3(MYH6):c.4823G>A (p.Arg1608His) rs747494958
NM_002471.3(MYH6):c.5077G>A (p.Val1693Met) rs373457153
NM_002471.3(MYH6):c.5137G>A (p.Glu1713Lys) rs369275573
NM_002471.3(MYH6):c.5267A>G (p.Lys1756Arg) rs746064687
NM_002471.3(MYH6):c.5410C>A (p.Gln1804Lys) rs144571463
NM_002471.3(MYH6):c.5458C>T (p.Arg1820Trp) rs111473291
NM_002471.3(MYH6):c.5519A>G (p.Lys1840Arg) rs373629059
NM_002471.3(MYH6):c.5696G>A (p.Arg1899His) rs61731171
NM_002471.3(MYH6):c.5710G>A (p.Glu1904Lys) rs1057518591
NM_002471.3(MYH6):c.5809G>A (p.Asp1937Asn) rs878854503
NM_002471.3(MYH6):c.831G>T (p.Gln277His) rs140660481

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