ClinVar Miner

List of variants in gene MYH6 reported as uncertain significance for Cardiovascular phenotype

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Total variants: 83
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HGVS dbSNP
NM_002471.3(MYH6):c.1007C>G (p.Ala336Gly) rs138572790
NM_002471.3(MYH6):c.1139A>C (p.Glu380Ala) rs747070258
NM_002471.3(MYH6):c.1154C>T (p.Ser385Leu) rs778319108
NM_002471.3(MYH6):c.1252G>A (p.Val418Met) rs147606900
NM_002471.3(MYH6):c.1336G>A (p.Ala446Thr) rs556536964
NM_002471.3(MYH6):c.1408G>A (p.Asp470Asn) rs777651128
NM_002471.3(MYH6):c.1410C>T (p.Asp470=) rs139886074
NM_002471.3(MYH6):c.1520T>C (p.Ile507Thr) rs188023690
NM_002471.3(MYH6):c.1753G>A (p.Gly585Ser) rs150415679
NM_002471.3(MYH6):c.1977del (p.Lys659fs) rs780949569
NM_002471.3(MYH6):c.2273A>G (p.Tyr758Cys) rs528854076
NM_002471.3(MYH6):c.2383C>T (p.Arg795Trp) rs202120238
NM_002471.3(MYH6):c.2430-4C>A rs376527296
NM_002471.3(MYH6):c.2440C>A (p.Leu814Met) rs150675144
NM_002471.3(MYH6):c.2554G>A (p.Ala852Thr) rs776971183
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.2722G>A (p.Asp908Asn) rs758061689
NM_002471.3(MYH6):c.2768A>C (p.Glu923Ala) rs371709369
NM_002471.3(MYH6):c.2771T>A (p.Met924Lys) rs746669440
NM_002471.3(MYH6):c.2928+5G>A rs28730772
NM_002471.3(MYH6):c.2928G>A (p.Lys976=) rs757078942
NM_002471.3(MYH6):c.2929-3C>T rs376752266
NM_002471.3(MYH6):c.2969T>A (p.Ile990Asn) rs766362714
NM_002471.3(MYH6):c.3010G>T (p.Ala1004Ser) rs143978652
NM_002471.3(MYH6):c.3049G>A (p.Asp1017Asn) rs1555333948
NM_002471.3(MYH6):c.3139C>T (p.Arg1047Cys) rs755565288
NM_002471.3(MYH6):c.3140G>A (p.Arg1047His) rs775843647
NM_002471.3(MYH6):c.3154C>T (p.Arg1052Ter) rs532606047
NM_002471.3(MYH6):c.3203T>C (p.Ile1068Thr) rs777320756
NM_002471.3(MYH6):c.3243G>T (p.Lys1081Asn) rs1555333894
NM_002471.3(MYH6):c.3343-3del rs1027186100
NM_002471.3(MYH6):c.3347G>A (p.Arg1116His) rs369247906
NM_002471.3(MYH6):c.3428G>A (p.Arg1143Gln) rs543585784
NM_002471.3(MYH6):c.3508G>A (p.Glu1170Lys) rs727503236
NM_002471.3(MYH6):c.3532C>T (p.Arg1178Trp) rs886039180
NM_002471.3(MYH6):c.3612G>C (p.Glu1204Asp) rs751153777
NM_002471.3(MYH6):c.3619G>A (p.Glu1207Lys) rs397516762
NM_002471.3(MYH6):c.3784C>T (p.Arg1262Cys) rs397516763
NM_002471.3(MYH6):c.3802G>A (p.Ala1268Thr) rs777331087
NM_002471.3(MYH6):c.3808C>T (p.Arg1270Cys) rs371849826
NM_002471.3(MYH6):c.3980C>T (p.Ala1327Val) rs148558068
NM_002471.3(MYH6):c.4016G>A (p.Arg1339Gln) rs766238876
NM_002471.3(MYH6):c.4047C>A (p.Tyr1349Ter) rs570555040
NM_002471.3(MYH6):c.4048G>A (p.Glu1350Lys) rs756392451
NM_002471.3(MYH6):c.4082G>A (p.Arg1361His) rs533942127
NM_002471.3(MYH6):c.4193G>A (p.Arg1398Gln) rs150815925
NM_002471.3(MYH6):c.4286A>T (p.Asp1429Val) rs755434984
NM_002471.3(MYH6):c.4325C>T (p.Ala1442Val) rs141534763
NM_002471.3(MYH6):c.4429C>T (p.Arg1477Cys) rs201989347
NM_002471.3(MYH6):c.4573G>A (p.Val1525Met) rs900579440
NM_002471.3(MYH6):c.4604T>G (p.Leu1535Arg) rs886039002
NM_002471.3(MYH6):c.4629G>C (p.Gln1543His) rs1177280918
NM_002471.3(MYH6):c.4651-4C>A rs766134513
NM_002471.3(MYH6):c.4685G>A (p.Arg1562Gln) rs371068881
NM_002471.3(MYH6):c.4721T>A (p.Ile1574Asn) rs199627411
NM_002471.3(MYH6):c.4723G>A (p.Glu1575Lys) rs371067114
NM_002471.3(MYH6):c.4747G>A (p.Glu1583Lys) rs397516771
NM_002471.3(MYH6):c.4819_4820AC[1] (p.Arg1608fs) rs764543612
NM_002471.3(MYH6):c.4907G>A (p.Arg1636His) rs746448302
NM_002471.3(MYH6):c.5137G>A (p.Glu1713Lys) rs369275573
NM_002471.3(MYH6):c.5141G>C (p.Arg1714Pro) rs777682189
NM_002471.3(MYH6):c.5183_5185AGA[3] (p.Lys1731del) rs886039114
NM_002471.3(MYH6):c.5201C>T (p.Ser1734Leu) rs151324358
NM_002471.3(MYH6):c.5293G>A (p.Ala1765Thr) rs397516775
NM_002471.3(MYH6):c.5297T>C (p.Met1766Thr) rs760667847
NM_002471.3(MYH6):c.5336C>A (p.Ala1779Asp) rs769271404
NM_002471.3(MYH6):c.5348G>A (p.Arg1783His) rs745473249
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.5476_5477delinsAA (p.Gly1826Asn) rs878854502
NM_002471.3(MYH6):c.5519A>G (p.Lys1840Arg) rs373629059
NM_002471.3(MYH6):c.5540G>A (p.Arg1847Gln) rs767679378
NM_002471.3(MYH6):c.5542C>T (p.Arg1848Cys) rs570853853
NM_002471.3(MYH6):c.5635G>A (p.Ala1879Thr) rs1457647629
NM_002471.3(MYH6):c.5660C>T (p.Ala1887Val) rs767096302
NM_002471.3(MYH6):c.5692T>G (p.Phe1898Val) rs762923098
NM_002471.3(MYH6):c.5767C>T (p.Arg1923Ter) rs765861895
NM_002471.3(MYH6):c.5809G>A (p.Asp1937Asn) rs878854503
NM_002471.3(MYH6):c.643-3T>C rs113552091
NM_002471.3(MYH6):c.643-5C>T rs199859986
NM_002471.3(MYH6):c.902T>C (p.Met301Thr) rs1555334802

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