List of variants reported as benign for Myopathy, centronuclear, 2 by Labcorp Genetics (formerly Invitae), Labcorp

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Total variants: 28

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HGVS	dbSNP	gnomAD frequency
NM_139343.3(BIN1):c.84+4287G>T	rs755639	0.56496
NM_139343.3(BIN1):c.698+10A>G	rs72481904	0.30545
NM_139343.3(BIN1):c.486T>C (p.Thr162=)	rs1060743	0.29063
NM_139343.3(BIN1):c.858-12C>A	rs6720741	0.20254
NM_139343.3(BIN1):c.957C>T (p.Ala319=)	rs2276579	0.13837
NM_139343.3(BIN1):c.775-4G>A	rs61748157	0.10181
NM_139343.3(BIN1):c.1573-18G>C	rs12466912	0.04714
NM_139343.3(BIN1):c.714C>T (p.Tyr238=)	rs1137845	0.04283
NM_139343.3(BIN1):c.894G>A (p.Ser298=)	rs2228955	0.03955
NM_139343.3(BIN1):c.1595C>T (p.Thr532Met)	rs112318500	0.03069
NM_139343.3(BIN1):c.1362G>T (p.Gly454=)	rs61748155	0.01414
NM_139343.3(BIN1):c.1263+11C>T	rs78967885	0.00935
NM_139343.3(BIN1):c.1625A>G (p.Lys542Arg)	rs138047593	0.00841
NM_139343.3(BIN1):c.1132-7T>C	rs115938552	0.00498
NM_139343.3(BIN1):c.888C>T (p.Ser296=)	rs114833236	0.00403
NM_139343.3(BIN1):c.1131+18C>T	rs191760397	0.00233
NM_139343.3(BIN1):c.858-5C>T	rs75328896	0.00222
NM_139343.3(BIN1):c.384G>A (p.Thr128=)	rs61748158	0.00203
NM_139343.3(BIN1):c.1540C>T (p.Arg514Cys)	rs148422103	0.00152
NM_139343.3(BIN1):c.1611C>T (p.Asp537=)	rs142523172	0.00101
NM_139343.3(BIN1):c.1003-15G>A	rs149290511	0.00095
NM_139343.3(BIN1):c.30G>A (p.Thr10=)	rs35535012	0.00067
NM_139343.3(BIN1):c.1292C>T (p.Pro431Leu)	rs141119288	0.00043
NM_139343.3(BIN1):c.1674+20G>A	rs374227714	0.00029
NM_139343.3(BIN1):c.316-19G>A	rs369840788	0.00018
NM_139343.3(BIN1):c.1131+9C>T	rs138606879	0.00005
NM_139343.3(BIN1):c.1003-16C>T	rs547659375	0.00003
NM_139343.3(BIN1):c.1132-22TGC[7]	rs748026377

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