ClinVar Miner

List of variants in gene MYH6 reported as likely benign for not specified

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Gene type:
ClinVar version:
Total variants: 134
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HGVS dbSNP
NM_002471.3(MYH6):c.*8T>C rs201560522
NM_002471.3(MYH6):c.1002+9G>A rs727504680
NM_002471.3(MYH6):c.1083G>T (p.Gly361=) rs138928022
NM_002471.3(MYH6):c.1122G>A (p.Ala374=) rs148091079
NM_002471.3(MYH6):c.1131C>G (p.Asp377Glu) rs61742472
NM_002471.3(MYH6):c.1131C>T (p.Asp377=) rs61742472
NM_002471.3(MYH6):c.1132G>A (p.Gly378Ser) rs148962966
NM_002471.3(MYH6):c.1141+11C>T rs373521230
NM_002471.3(MYH6):c.1141+8G>T rs377327277
NM_002471.3(MYH6):c.1155G>A (p.Ser385=) rs147903010
NM_002471.3(MYH6):c.1252G>A (p.Val418Met) rs147606900
NM_002471.3(MYH6):c.1275C>T (p.Ile425=) rs61742470
NM_002471.3(MYH6):c.1383G>A (p.Leu461=) rs1057523926
NM_002471.3(MYH6):c.1410C>T (p.Asp470=) rs139886074
NM_002471.3(MYH6):c.1581+10delT rs560271582
NM_002471.3(MYH6):c.1581+19C>G rs201495432
NM_002471.3(MYH6):c.1582-7C>T rs374941865
NM_002471.3(MYH6):c.1662C>T (p.Tyr554=) rs374114140
NM_002471.3(MYH6):c.1734C>T (p.Phe578=) rs1057523847
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.1779C>A (p.Gly593=) rs190996339
NM_002471.3(MYH6):c.1809C>T (p.Asn603=) rs186134696
NM_002471.3(MYH6):c.1839C>G (p.Ser613=) rs138984258
NM_002471.3(MYH6):c.1875C>T (p.Tyr625=) rs146591697
NM_002471.3(MYH6):c.1935C>T (p.Ser645=) rs142393002
NM_002471.3(MYH6):c.1944G>A (p.Thr648=) rs367742240
NM_002471.3(MYH6):c.1960C>A (p.Arg654=) rs369938365
NM_002471.3(MYH6):c.1989C>T (p.Asn663=) rs28730774
NM_002471.3(MYH6):c.2071G>A (p.Val691Ile) rs148915045
NM_002471.3(MYH6):c.2097C>T (p.Gly699=) rs149734381
NM_002471.3(MYH6):c.2127G>A (p.Lys709=) rs765316931
NM_002471.3(MYH6):c.2199T>C (p.Pro733=) rs727505290
NM_002471.3(MYH6):c.2293-12C>G rs115453571
NM_002471.3(MYH6):c.2293-19A>G rs375891567
NM_002471.3(MYH6):c.2429+14A>C rs200817451
NM_002471.3(MYH6):c.2430-14C>T rs190342289
NM_002471.3(MYH6):c.2430-4C>A rs376527296
NM_002471.3(MYH6):c.2430-8C>G rs201624129
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.2541G>A (p.Thr847=) rs774131751
NM_002471.3(MYH6):c.2685+14A>T rs765118655
NM_002471.3(MYH6):c.2721C>T (p.Cys907=) rs1014932127
NM_002471.3(MYH6):c.2805C>T (p.Asn935=) rs757958461
NM_002471.3(MYH6):c.2890G>T (p.Ala964Ser) rs144907522
NM_002471.3(MYH6):c.2928+5G>A rs28730772
NM_002471.3(MYH6):c.2973C>T (p.Ile991=) rs374807345
NM_002471.3(MYH6):c.3010G>T (p.Ala1004Ser) rs143978652
NM_002471.3(MYH6):c.3118C>T (p.Leu1040=) rs368497504
NM_002471.3(MYH6):c.3177C>T (p.Gly1059=) rs529676901
NM_002471.3(MYH6):c.3199A>G (p.Ser1067Gly) rs145508517
NM_002471.3(MYH6):c.3234G>A (p.Leu1078=) rs149682518
NM_002471.3(MYH6):c.3297G>A (p.Glu1099=) rs144957142
NM_002471.3(MYH6):c.3303G>A (p.Val1101=) rs143825034
NM_002471.3(MYH6):c.3342+10T>C rs552662475
NM_002471.3(MYH6):c.3343-3delC rs1027186100
NM_002471.3(MYH6):c.3369G>A (p.Glu1123=) rs876657517
NM_002471.3(MYH6):c.3378C>T (p.Ala1126=) rs752939591
NM_002471.3(MYH6):c.3393G>A (p.Arg1131=) rs529107714
NM_002471.3(MYH6):c.3417A>G (p.Ser1139=) rs1057523683
NM_002471.3(MYH6):c.3420C>T (p.Asp1140=) rs1057523901
NM_002471.3(MYH6):c.3489C>A (p.Ile1163=) rs764540332
NM_002471.3(MYH6):c.3573C>T (p.Ala1191=) rs727505358
NM_002471.3(MYH6):c.3636G>A (p.Leu1212=) rs774392020
NM_002471.3(MYH6):c.3732+13C>T rs369889994
NM_002471.3(MYH6):c.3787G>A (p.Val1263Met) rs375819633
NM_002471.3(MYH6):c.3852C>T (p.Thr1284=) rs141143152
NM_002471.3(MYH6):c.3860-12T>C rs937933268
NM_002471.3(MYH6):c.3860-15T>G rs200883903
NM_002471.3(MYH6):c.3883G>C (p.Glu1295Gln) rs34935550
NM_002471.3(MYH6):c.3903G>A (p.Ser1301=) rs201804323
NM_002471.3(MYH6):c.3927T>C (p.Ser1309=) rs115742584
NM_002471.3(MYH6):c.3978+8C>T rs367866050
NM_002471.3(MYH6):c.3979-10C>A rs28730768
NM_002471.3(MYH6):c.3979-10C>T rs28730768
NM_002471.3(MYH6):c.3979-11_3979-9delCCCinsG rs368229372
NM_002471.3(MYH6):c.3979-13C>A rs563648655
NM_002471.3(MYH6):c.3979-13C>G rs563648655
NM_002471.3(MYH6):c.3979-14C>A rs372226248
NM_002471.3(MYH6):c.3979-14C>G rs372226248
NM_002471.3(MYH6):c.3979-14C>T rs372226248
NM_002471.3(MYH6):c.3979-15_3979-14delCCinsA rs1555333587
NM_002471.3(MYH6):c.3979-7delTinsGC rs545343612
NM_002471.3(MYH6):c.3979-8_3979-7delinsGC rs727503235
NM_002471.3(MYH6):c.4125C>G (p.Thr1375=) rs876657518
NM_002471.3(MYH6):c.4136C>T (p.Thr1379Met) rs145611185
NM_002471.3(MYH6):c.4137G>A (p.Thr1379=) rs372158844
NM_002471.3(MYH6):c.4185G>A (p.Leu1395=) rs1555333480
NM_002471.3(MYH6):c.4320T>A (p.Ala1440=) rs145566711
NM_002471.3(MYH6):c.4359+20C>T rs770770450
NM_002471.3(MYH6):c.4359+5_4359+8delACCAinsGCCC rs1064795890
NM_002471.3(MYH6):c.4401T>G (p.Ser1467=) rs150081280
NM_002471.3(MYH6):c.4416A>G (p.Ser1472=) rs140800076
NM_002471.3(MYH6):c.4470C>T (p.Tyr1490=) rs727504964
NM_002471.3(MYH6):c.4525+13T>C rs397516770
NM_002471.3(MYH6):c.4525+6C>T rs1057523902
NM_002471.3(MYH6):c.4536G>A (p.Ser1512=) rs142539180
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.4782G>A (p.Arg1594=) rs142823394
NM_002471.3(MYH6):c.4812T>C (p.Asp1604=) rs201667127
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.4959+12C>T rs371661383
NM_002471.3(MYH6):c.4986G>A (p.Ala1662=) rs77416370
NM_002471.3(MYH6):c.5019C>T (p.Ile1673=) rs397516773
NM_002471.3(MYH6):c.5112G>A (p.Ala1704=) rs150450178
NM_002471.3(MYH6):c.5136C>T (p.Ser1712=) rs397516774
NM_002471.3(MYH6):c.5163+3G>A rs1057524287
NM_002471.3(MYH6):c.5271C>T (p.Ala1757=) rs1239601327
NM_002471.3(MYH6):c.5290-11C>G rs764779081
NM_002471.3(MYH6):c.5400C>T (p.Asp1800=) rs144329079
NM_002471.3(MYH6):c.5439G>A (p.Gln1813=) rs200854143
NM_002471.3(MYH6):c.5490C>T (p.Ala1830=) rs201209864
NM_002471.3(MYH6):c.5505C>T (p.Asn1835=) rs549746895
NM_002471.3(MYH6):c.5514G>T (p.Ser1838=) rs727503232
NM_002471.3(MYH6):c.5566-7C>T rs200509899
NM_002471.3(MYH6):c.5601G>A (p.Gln1867=) rs148984154
NM_002471.3(MYH6):c.5652C>T (p.Ala1884=) rs200662317
NM_002471.3(MYH6):c.643-5C>T rs199859986
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.736-9C>T rs748594445
NM_002471.3(MYH6):c.799+10A>C rs774371819
NM_002471.3(MYH6):c.799+14G>C rs727505139
NM_002471.3(MYH6):c.800-5C>T rs727505228
NM_002471.3(MYH6):c.831G>T (p.Gln277His) rs140660481
NM_002471.3(MYH6):c.898+6C>A rs370158816
NM_002471.3(MYH6):c.898+6C>T rs370158816
NM_002471.3(MYH6):c.981C>T (p.Ser327=) rs148407931

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