List of variants reported as benign for Myofibrillar myopathy 3

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Total variants: 22

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HGVS	dbSNP	gnomAD frequency
NM_006790.3(MYOT):c.220= (p.Gln74=)	rs6890689	0.98540
NM_006790.3(MYOT):c.*98G>A	rs4288	0.10310
NM_006790.3(MYOT):c.149A>G (p.Gln50Arg)	rs34717730	0.02506
NM_006790.3(MYOT):c.-251A>G	rs6863775	0.01894
NM_006790.3(MYOT):c.*190C>G	rs74711051	0.01853
NM_006790.3(MYOT):c.780G>A (p.Ser260=)	rs116773838	0.01617
NM_006790.3(MYOT):c.1008G>T (p.Val336=)	rs142828368	0.00381
NM_006790.3(MYOT):c.1190+7T>C	rs192405601	0.00311
NM_006790.3(MYOT):c.822T>C (p.Ser274=)	rs138678049	0.00195
NM_006790.3(MYOT):c.445G>C (p.Glu149Gln)	rs71578935	0.00152
NM_006790.3(MYOT):c.634-15T>C	rs115598221	0.00082
NM_006790.3(MYOT):c.-233C>A	rs186433387	0.00069
NM_006790.3(MYOT):c.1190+12A>G	rs183456886	0.00055
NM_006790.3(MYOT):c.*404G>A	rs188240755	0.00051
NM_006790.3(MYOT):c.*463C>T	rs149535236	0.00051
NM_006790.3(MYOT):c.617G>A (p.Gly206Asp)	rs151094883	0.00028
NM_006790.3(MYOT):c.323A>C (p.Asn108Thr)	rs142416150	0.00019
NM_006790.3(MYOT):c.533G>A (p.Arg178His)	rs150293853	0.00011
NM_006790.3(MYOT):c.1025-19T>A	rs762927139	0.00001
NM_006790.3(MYOT):c.1325-4T>A	rs544136408	0.00001
NM_006790.3(MYOT):c.630G>A (p.Ser210=)	rs375308029	0.00001
NM_006790.3(MYOT):c.240C>T (p.Asn80=)	rs529067126

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