ClinVar Miner

List of variants in gene MYH6 reported as likely benign for Cardiovascular phenotype

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Total variants: 56
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HGVS dbSNP
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.1185C>T (p.Asp395=) rs201822160
NM_002471.3(MYH6):c.1275C>T (p.Ile425=) rs61742470
NM_002471.3(MYH6):c.1485C>T (p.Phe495=) rs181613656
NM_002471.3(MYH6):c.1521T>C (p.Ile507=) rs142410102
NM_002471.3(MYH6):c.1599C>T (p.Ser533=) rs371263768
NM_002471.3(MYH6):c.1659G>A (p.Leu553=) rs763167861
NM_002471.3(MYH6):c.1662C>T (p.Tyr554=) rs374114140
NM_002471.3(MYH6):c.1860T>G (p.Thr620=) rs562851085
NM_002471.3(MYH6):c.1875C>T (p.Tyr625=) rs146591697
NM_002471.3(MYH6):c.1950G>A (p.Ser650=) rs752964239
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.2364G>A (p.Thr788=) rs779838927
NM_002471.3(MYH6):c.2367C>T (p.Arg789=) rs1343754890
NM_002471.3(MYH6):c.2401A>G (p.Ile801Val) rs75487328
NM_002471.3(MYH6):c.2574C>T (p.Phe858=) rs148596692
NM_002471.3(MYH6):c.2841C>T (p.Asp947=) rs140305424
NM_002471.3(MYH6):c.2890G>T (p.Ala964Ser) rs144907522
NM_002471.3(MYH6):c.2994G>A (p.Lys998=) rs1555333952
NM_002471.3(MYH6):c.3177C>T (p.Gly1059=) rs529676901
NM_002471.3(MYH6):c.3297G>A (p.Glu1099=) rs144957142
NM_002471.3(MYH6):c.3302_3303invTG (p.Val1101Ala)
NM_002471.3(MYH6):c.3468C>T (p.Gly1156=) rs545420992
NM_002471.3(MYH6):c.3573C>T (p.Ala1191=) rs727505358
NM_002471.3(MYH6):c.3591G>A (p.Lys1197=) rs886038871
NM_002471.3(MYH6):c.3798A>G (p.Glu1266=) rs756915746
NM_002471.3(MYH6):c.3903G>A (p.Ser1301=) rs201804323
NM_002471.3(MYH6):c.4026C>T (p.Cys1342=) rs141062252
NM_002471.3(MYH6):c.4047C>T (p.Tyr1349=) rs570555040
NM_002471.3(MYH6):c.4134G>A (p.Glu1378=) rs1555333539
NM_002471.3(MYH6):c.4137G>A (p.Thr1379=) rs372158844
NM_002471.3(MYH6):c.4293G>A (p.Met1431Ile) rs201016285
NM_002471.3(MYH6):c.4347A>G (p.Arg1449=) rs750834664
NM_002471.3(MYH6):c.4353T>C (p.Phe1451=) rs1555333457
NM_002471.3(MYH6):c.4365G>T (p.Leu1455=) rs779591168
NM_002471.3(MYH6):c.4401T>C (p.Ser1467=) rs150081280
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.4504C>A (p.Arg1502=) rs773631723
NM_002471.3(MYH6):c.4536G>A (p.Ser1512=) rs142539180
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.4833C>T (p.Asn1611=) rs139329956
NM_002471.3(MYH6):c.4905C>T (p.Asn1635=) rs143048583
NM_002471.3(MYH6):c.5112G>A (p.Ala1704=) rs150450178
NM_002471.3(MYH6):c.5544C>T (p.Arg1848=) rs147348589
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.678C>T (p.Pro226=) rs768893926
NM_002471.3(MYH6):c.679G>A (p.Ala227Thr) rs201828188

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