ClinVar Miner

List of variants in gene MYH6 reported as likely benign by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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Gene type:
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Total variants: 20
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HGVS dbSNP gnomAD frequency
NM_002471.4(MYH6):c.2579G>A (p.Arg860His) rs115845031 0.00573
NM_002471.4(MYH6):c.2071G>A (p.Val691Ile) rs148915045 0.00284
NM_002471.4(MYH6):c.1275C>T (p.Ile425=) rs61742470 0.00232
NM_002471.4(MYH6):c.3979-7dup rs545343612 0.00208
NM_002471.4(MYH6):c.4320T>A (p.Ala1440=) rs145566711 0.00189
NM_002471.4(MYH6):c.2928+5G>A rs28730772 0.00172
NM_002471.4(MYH6):c.1763A>C (p.Asp588Ala) rs142992009 0.00153
NM_002471.4(MYH6):c.2890G>T (p.Ala964Ser) rs144907522 0.00148
NM_002471.4(MYH6):c.3010G>T (p.Ala1004Ser) rs143978652 0.00110
NM_002471.4(MYH6):c.1083G>T (p.Gly361=) rs138928022 0.00092
NM_002471.4(MYH6):c.3573C>T (p.Ala1191=) rs727505358 0.00054
NM_002471.4(MYH6):c.4136C>T (p.Thr1379Met) rs145611185 0.00036
NM_002471.4(MYH6):c.4526-9G>C rs201785356 0.00013
NM_002471.4(MYH6):c.2929-3C>T rs376752266 0.00011
NM_002471.4(MYH6):c.4650+10G>A rs760975924 0.00005
NM_002471.4(MYH6):c.4140C>T (p.Asp1380=) rs199672166 0.00003
NM_002471.4(MYH6):c.5472G>A (p.Leu1824=) rs1890959581 0.00001
NM_002471.4(MYH6):c.5553G>A (p.Glu1851=) rs763313787 0.00001
NM_002471.4(MYH6):c.3979-10C>T rs28730768
NM_002471.4(MYH6):c.898+6C>T rs370158816

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