ClinVar Miner

List of variants in gene MYH6 reported as likely benign by Invitae

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Gene type:
ClinVar version:
Total variants: 97
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HGVS dbSNP
NM_002471.3(MYH6):c.1087A>T (p.Met363Leu) rs202196487
NM_002471.3(MYH6):c.1141+8G>C rs377327277
NM_002471.3(MYH6):c.1252G>A (p.Val418Met) rs147606900
NM_002471.3(MYH6):c.1368C>T (p.Tyr456=) rs1060504231
NM_002471.3(MYH6):c.1381C>T (p.Leu461=) rs368609214
NM_002471.3(MYH6):c.1398C>T (p.Phe466=) rs745448722
NM_002471.3(MYH6):c.1485C>T (p.Phe495=) rs181613656
NM_002471.3(MYH6):c.1581+10delT rs560271582
NM_002471.3(MYH6):c.1582-7C>T rs374941865
NM_002471.3(MYH6):c.1599C>T (p.Ser533=) rs371263768
NM_002471.3(MYH6):c.1749C>T (p.Tyr583=) rs187508349
NM_002471.3(MYH6):c.1752C>T (p.Ala584=) rs756971568
NM_002471.3(MYH6):c.1763A>C (p.Asp588Ala) rs142992009
NM_002471.3(MYH6):c.1875C>T (p.Tyr625=) rs146591697
NM_002471.3(MYH6):c.2067C>T (p.Pro689=) rs775834885
NM_002471.3(MYH6):c.2097C>T (p.Gly699=) rs149734381
NM_002471.3(MYH6):c.2250T>C (p.Ser750=) rs144050960
NM_002471.3(MYH6):c.2322G>A (p.Leu774=) rs1555334170
NM_002471.3(MYH6):c.2430-4C>A rs376527296
NM_002471.3(MYH6):c.2464G>A (p.Ala822Thr) rs138419275
NM_002471.3(MYH6):c.2520G>A (p.Pro840=) rs141945051
NM_002471.3(MYH6):c.2521C>T (p.Leu841=) rs760142743
NM_002471.3(MYH6):c.2614C>T (p.Arg872Cys) rs201193346
NM_002471.3(MYH6):c.2685+10C>T rs202155137
NM_002471.3(MYH6):c.2805C>T (p.Asn935=) rs757958461
NM_002471.3(MYH6):c.2844G>A (p.Glu948=) rs1400491977
NM_002471.3(MYH6):c.2928+5G>A rs28730772
NM_002471.3(MYH6):c.3010G>T (p.Ala1004Ser) rs143978652
NM_002471.3(MYH6):c.3105+9T>C rs1555333942
NM_002471.3(MYH6):c.3118C>T (p.Leu1040=) rs368497504
NM_002471.3(MYH6):c.3164G>A (p.Arg1055Gln) rs540893860
NM_002471.3(MYH6):c.3195G>C (p.Gln1065His) rs267606904
NM_002471.3(MYH6):c.3230A>T (p.Gln1077Leu) rs377716628
NM_002471.3(MYH6):c.3342+10T>C rs552662475
NM_002471.3(MYH6):c.3343-3delC rs1027186100
NM_002471.3(MYH6):c.3378C>T (p.Ala1126=) rs752939591
NM_002471.3(MYH6):c.3465C>T (p.Ala1155=) rs749057068
NM_002471.3(MYH6):c.3477G>A (p.Thr1159=) rs573242724
NM_002471.3(MYH6):c.3489C>T (p.Ile1163=) rs764540332
NM_002471.3(MYH6):c.3540G>A (p.Leu1180=) rs778853343
NM_002471.3(MYH6):c.3597C>T (p.Ala1199=) rs1269257633
NM_002471.3(MYH6):c.3609C>T (p.Ala1203=) rs149369904
NM_002471.3(MYH6):c.3634C>T (p.Leu1212=) rs1053714593
NM_002471.3(MYH6):c.3759G>T (p.Thr1253=) rs761754298
NM_002471.3(MYH6):c.3860-8A>G rs772882288
NM_002471.3(MYH6):c.3876G>A (p.Gln1292=) rs145290322
NM_002471.3(MYH6):c.3903G>A (p.Ser1301=) rs201804323
NM_002471.3(MYH6):c.3979-10C>A rs28730768
NM_002471.3(MYH6):c.3979-10C>G rs28730768
NM_002471.3(MYH6):c.3979-10C>T rs28730768
NM_002471.3(MYH6):c.3979-10_3979-8delCCC rs193922652
NM_002471.3(MYH6):c.3979-7T>G rs535111647
NM_002471.3(MYH6):c.3979-7_3979-5delTCC rs397516764
NM_002471.3(MYH6):c.3979-8_3979-7delinsGC rs727503235
NM_002471.3(MYH6):c.4027G>A (p.Asp1343Asn) rs761711033
NM_002471.3(MYH6):c.4071C>T (p.Ala1357=) rs147328051
NM_002471.3(MYH6):c.4104G>A (p.Ser1368=) rs374887637
NM_002471.3(MYH6):c.4136C>T (p.Thr1379Met) rs145611185
NM_002471.3(MYH6):c.4140C>T (p.Asp1380=) rs199672166
NM_002471.3(MYH6):c.4245A>G (p.Ser1415=) rs779697115
NM_002471.3(MYH6):c.4265G>A (p.Arg1422Gln) rs574433291
NM_002471.3(MYH6):c.4299C>T (p.Asp1433=) rs765006624
NM_002471.3(MYH6):c.4359+10G>A rs368183862
NM_002471.3(MYH6):c.4359+8A>C rs188675676
NM_002471.3(MYH6):c.4365G>T (p.Leu1455=) rs779591168
NM_002471.3(MYH6):c.4401T>G (p.Ser1467=) rs150081280
NM_002471.3(MYH6):c.4505G>A (p.Arg1502Gln) rs199936506
NM_002471.3(MYH6):c.4560A>G (p.Glu1520=) rs200918670
NM_002471.3(MYH6):c.4595G>T (p.Arg1532Leu) rs34330111
NM_002471.3(MYH6):c.4611G>A (p.Val1537=) rs142983918
NM_002471.3(MYH6):c.4650+10G>A rs760975924
NM_002471.3(MYH6):c.4650+9C>T rs764593204
NM_002471.3(MYH6):c.4833C>T (p.Asn1611=) rs139329956
NM_002471.3(MYH6):c.4905C>T (p.Asn1635=) rs143048583
NM_002471.3(MYH6):c.4906C>T (p.Arg1636Cys) rs149460065
NM_002471.3(MYH6):c.5001C>T (p.Asp1667=) rs377698958
NM_002471.3(MYH6):c.5112G>A (p.Ala1704=) rs150450178
NM_002471.3(MYH6):c.5133C>G (p.Thr1711=) rs775234352
NM_002471.3(MYH6):c.5140C>A (p.Arg1714=) rs140651265
NM_002471.3(MYH6):c.5251A>C (p.Arg1751=) rs1555333151
NM_002471.3(MYH6):c.5367G>A (p.Glu1789=) rs753335327
NM_002471.3(MYH6):c.5403G>A (p.Glu1801=) rs762151922
NM_002471.3(MYH6):c.5410C>A (p.Gln1804Lys) rs144571463
NM_002471.3(MYH6):c.5514G>T (p.Ser1838=) rs727503232
NM_002471.3(MYH6):c.5553G>A (p.Glu1851=) rs763313787
NM_002471.3(MYH6):c.5566-7C>T rs200509899
NM_002471.3(MYH6):c.5661+9A>G rs373908250
NM_002471.3(MYH6):c.643-5C>T rs199859986
NM_002471.3(MYH6):c.651G>A (p.Leu217=) rs1262690268
NM_002471.3(MYH6):c.678C>T (p.Pro226=) rs768893926
NM_002471.3(MYH6):c.732C>T (p.Arg244=) rs397516779
NM_002471.3(MYH6):c.735+10T>C rs1555334939
NM_002471.3(MYH6):c.736-9C>T rs748594445
NM_002471.3(MYH6):c.800-5C>T rs727505228
NM_002471.3(MYH6):c.824T>A (p.Ile275Asn) rs201327273
NM_002471.3(MYH6):c.831G>T (p.Gln277His) rs140660481
NM_002471.3(MYH6):c.888G>A (p.Pro296=) rs765433125

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