ClinVar Miner

List of variants in gene MYH6 reported as uncertain significance for not provided

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Gene type:
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Total variants: 77
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HGVS dbSNP
NM_002471.3(MYH6):c.1139A>C (p.Glu380Ala) rs747070258
NM_002471.3(MYH6):c.1177T>G (p.Ser393Ala) rs199877580
NM_002471.3(MYH6):c.1252G>A (p.Val418Met) rs147606900
NM_002471.3(MYH6):c.1328G>A (p.Arg443His) rs202096001
NM_002471.3(MYH6):c.1373T>C (p.Ile458Thr) rs774807696
NM_002471.3(MYH6):c.1410C>T (p.Asp470=) rs139886074
NM_002471.3(MYH6):c.1521T>G (p.Ile507Met) rs142410102
NM_002471.3(MYH6):c.1610A>G (p.Glu537Gly) rs1555334438
NM_002471.3(MYH6):c.1628A>G (p.Lys543Arg) rs367663906
NM_002471.3(MYH6):c.1716dup (p.Lys573fs) rs786205354
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.2217T>C (p.Asp739=) rs374177807
NM_002471.3(MYH6):c.2353C>T (p.Arg785Cys)
NM_002471.3(MYH6):c.2575G>T (p.Gly859Trp) rs369274077
NM_002471.3(MYH6):c.2578C>A (p.Arg860Ser) rs1025146248
NM_002471.3(MYH6):c.2578C>T (p.Arg860Cys) 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.3010G>T (p.Ala1004Ser) rs143978652
NM_002471.3(MYH6):c.3105+9T>C rs1555333942
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.3327A>G (p.Lys1109=) rs755818414
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.3437dup (p.Glu1147fs) rs397516761
NM_002471.3(MYH6):c.3448G>A (p.Glu1150Lys) rs760399050
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.3604G>A (p.Val1202Met) rs368451573
NM_002471.3(MYH6):c.3672C>G (p.Ser1224Arg) rs755267212
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.3817A>T (p.Asn1273Tyr) rs200503588
NM_002471.3(MYH6):c.3835C>T (p.Arg1279Ter) rs751426149
NM_002471.3(MYH6):c.3988G>A (p.Ala1330Thr) rs757840030
NM_002471.3(MYH6):c.4015C>T (p.Arg1339Trp) rs985894009
NM_002471.3(MYH6):c.4016G>A (p.Arg1339Gln) rs766238876
NM_002471.3(MYH6):c.4026C>A (p.Cys1342Ter) rs141062252
NM_002471.3(MYH6):c.4140C>A (p.Asp1380Glu) rs199672166
NM_002471.3(MYH6):c.4150C>T (p.Arg1384Trp) rs763926580
NM_002471.3(MYH6):c.4193G>A (p.Arg1398Gln) rs150815925
NM_002471.3(MYH6):c.4394C>T (p.Ser1465Leu) rs766327056
NM_002471.3(MYH6):c.4429C>T (p.Arg1477Cys) rs201989347
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.4772A>G (p.Asn1591Ser) rs200751434
NM_002471.3(MYH6):c.4822C>T (p.Arg1608Cys) rs201683868
NM_002471.3(MYH6):c.4905C>T (p.Asn1635=) rs143048583
NM_002471.3(MYH6):c.4999G>A (p.Asp1667Asn) rs758251388
NM_002471.3(MYH6):c.5036G>T (p.Arg1679Leu) rs483352719
NM_002471.3(MYH6):c.5135G>T (p.Ser1712Ile) rs201383498
NM_002471.3(MYH6):c.5137G>A (p.Glu1713Lys) rs369275573
NM_002471.3(MYH6):c.5140C>T (p.Arg1714Trp) rs140651265
NM_002471.3(MYH6):c.5267A>G (p.Lys1756Arg) rs746064687
NM_002471.3(MYH6):c.5393G>A (p.Arg1798Gln) rs759281871
NM_002471.3(MYH6):c.5400C>T (p.Asp1800=) rs144329079
NM_002471.3(MYH6):c.5458C>T (p.Arg1820Trp) rs111473291
NM_002471.3(MYH6):c.5491G>A (p.Glu1831Lys) rs367834703
NM_002471.3(MYH6):c.5513C>T (p.Ser1838Leu) rs747673552
NM_002471.3(MYH6):c.5519A>G (p.Lys1840Arg) rs373629059
NM_002471.3(MYH6):c.5566-9C>T rs758869144
NM_002471.3(MYH6):c.5652C>T (p.Ala1884=) rs200662317
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.731G>A (p.Arg244His) rs200645920
NM_002471.3(MYH6):c.831G>T (p.Gln277His) rs140660481

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