ClinVar Miner

List of variants in gene MYH6 reported as likely benign by Laboratory for Molecular Medicine,Partners HealthCare Personalized Medicine

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Gene type:
ClinVar version:
Total variants: 55
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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+8G>T rs377327277
NM_002471.3(MYH6):c.1410C>T (p.Asp470=) rs139886074
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.2071G>A (p.Val691Ile) rs148915045
NM_002471.3(MYH6):c.2097C>T (p.Gly699=) rs149734381
NM_002471.3(MYH6):c.2199T>C (p.Pro733=) rs727505290
NM_002471.3(MYH6):c.2293-12C>G rs115453571
NM_002471.3(MYH6):c.2429+14A>C rs200817451
NM_002471.3(MYH6):c.2430-14C>T rs190342289
NM_002471.3(MYH6):c.2464G>A (p.Ala822Thr) rs138419275
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.3010G>T (p.Ala1004Ser) rs143978652
NM_002471.3(MYH6):c.3118C>T (p.Leu1040=) rs368497504
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.3369G>A (p.Glu1123=) rs876657517
NM_002471.3(MYH6):c.3393G>A (p.Arg1131=) rs529107714
NM_002471.3(MYH6):c.3573C>T (p.Ala1191=) rs727505358
NM_002471.3(MYH6):c.3787G>A (p.Val1263Met) rs375819633
NM_002471.3(MYH6):c.3903G>A (p.Ser1301=) rs201804323
NM_002471.3(MYH6):c.3978+8C>T rs367866050
NM_002471.3(MYH6):c.4125C>G (p.Thr1375=) rs876657518
NM_002471.3(MYH6):c.4137G>A (p.Thr1379=) rs372158844
NM_002471.3(MYH6):c.4401T>G (p.Ser1467=) rs150081280
NM_002471.3(MYH6):c.4470C>T (p.Tyr1490=) rs727504964
NM_002471.3(MYH6):c.4525+13T>C rs397516770
NM_002471.3(MYH6):c.4536G>A (p.Ser1512=) rs142539180
NM_002471.3(MYH6):c.4611G>A (p.Val1537=) rs142983918
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.5439G>A (p.Gln1813=) rs200854143
NM_002471.3(MYH6):c.5514G>T (p.Ser1838=) rs727503232
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+14G>C rs727505139
NM_002471.3(MYH6):c.800-5C>T rs727505228
NM_002471.3(MYH6):c.981C>T (p.Ser327=) rs148407931

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