ClinVar Miner

List of variants in gene MYH6 reported as likely benign for Cardiomyopathy

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Total variants: 44
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HGVS dbSNP gnomAD frequency
NM_002471.4(MYH6):c.3627C>T (p.Ile1209=) rs147871745 0.00930
NM_002471.4(MYH6):c.2579G>A (p.Arg860His) rs115845031 0.00573
NM_002471.4(MYH6):c.4320T>A (p.Ala1440=) rs145566711 0.00189
NM_002471.4(MYH6):c.3927T>C (p.Ser1309=) rs115742584 0.00145
NM_002471.4(MYH6):c.3010G>T (p.Ala1004Ser) rs143978652 0.00110
NM_002471.4(MYH6):c.3903G>A (p.Ser1301=) rs201804323 0.00052
NM_002471.4(MYH6):c.4193G>A (p.Arg1398Gln) rs150815925 0.00041
NM_002471.4(MYH6):c.643-5C>T rs199859986 0.00041
NM_002471.4(MYH6):c.4611G>A (p.Val1537=) rs142983918 0.00030
NM_002471.4(MYH6):c.2685+10C>T rs202155137 0.00024
NM_002471.4(MYH6):c.4359+10G>A rs368183862 0.00024
NM_002471.4(MYH6):c.2430-4C>A rs376527296 0.00023
NM_002471.4(MYH6):c.1132G>A (p.Gly378Ser) rs148962966 0.00014
NM_002471.4(MYH6):c.1252G>A (p.Val418Met) rs147606900 0.00013
NM_002471.4(MYH6):c.2097C>T (p.Gly699=) rs149734381 0.00011
NM_002471.4(MYH6):c.2805C>T (p.Asn935=) rs757958461 0.00011
NM_002471.4(MYH6):c.5514G>T (p.Ser1838=) rs727503232 0.00010
NM_002471.4(MYH6):c.1935C>T (p.Ser645=) rs142393002 0.00009
NM_002471.4(MYH6):c.3178G>A (p.Asp1060Asn) rs775560235 0.00008
NM_002471.4(MYH6):c.3867G>T (p.Leu1289Phe) rs138127105 0.00008
NM_002471.4(MYH6):c.4164C>T (p.Leu1388=) rs201379347 0.00004
NM_002471.4(MYH6):c.4140C>T (p.Asp1380=) rs199672166 0.00003
NM_002471.4(MYH6):c.3576G>A (p.Ala1192=) rs762573185 0.00002
NM_002471.4(MYH6):c.693C>T (p.Phe231=) rs772154148 0.00002
NM_002471.4(MYH6):c.933C>T (p.Tyr311=) rs371728824 0.00002
NM_002471.4(MYH6):c.1200G>A (p.Leu400=) rs765041539 0.00001
NM_002471.4(MYH6):c.1486G>A (p.Val496Met) rs761085263 0.00001
NM_002471.4(MYH6):c.3513C>T (p.Ala1171=) rs773749966 0.00001
NM_002471.4(MYH6):c.5445G>A (p.Gln1815=) rs979327556 0.00001
NM_002471.4(MYH6):c.5508A>G (p.Ala1836=) rs193922654 0.00001
NM_002471.4(MYH6):c.1065A>C (p.Gly355=) rs2138615175
NM_002471.4(MYH6):c.1131C>G (p.Asp377Glu) rs61742472
NM_002471.4(MYH6):c.1131C>T (p.Asp377=) rs61742472
NM_002471.4(MYH6):c.2806G>T (p.Ala936Ser) rs141704264
NM_002471.4(MYH6):c.3428G>A (p.Arg1143Gln) rs543585784
NM_002471.4(MYH6):c.3447C>G (p.Ser1149Arg) rs564367705
NM_002471.4(MYH6):c.3682C>T (p.Leu1228=) rs1033363939
NM_002471.4(MYH6):c.3979-10C>A rs28730768
NM_002471.4(MYH6):c.3979-7_3979-4del rs745326238
NM_002471.4(MYH6):c.3979-7_3979-5del rs397516764
NM_002471.4(MYH6):c.3979-8del rs193922652
NM_002471.4(MYH6):c.3979-9C>A rs57660219
NM_002471.4(MYH6):c.4595G>T (p.Arg1532Leu) rs34330111
NM_002471.4(MYH6):c.5476_5477delinsAA (p.Gly1826Asn) rs878854502

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