List of variants reported as likely benign for Nemaline myopathy 2 by Counsyl

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Total variants: 13

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HGVS	dbSNP
NM_001271208.1(NEB):c.23940+17_23940+21del	rs768100915
NM_001271208.2(NEB):c.11729A>G (p.Asp3910Gly)	rs35740585
NM_001271208.2(NEB):c.19102-31_19102-30del	rs774225336
NM_001271208.2(NEB):c.22077G>A (p.Lys7359=)	rs267598918
NM_001271208.2(NEB):c.22378-36CT[5]	rs751597547
NM_001271208.2(NEB):c.22533C>T (p.Leu7511=)	rs371431256
NM_001271208.2(NEB):c.23233-18del	rs1553616477
NM_001271208.2(NEB):c.23346+16C>T	rs75221580
NM_001271208.2(NEB):c.24312G>A (p.Ser8104=)	rs763193315
NM_001271208.2(NEB):c.3879+8G>A	rs376511134
NM_001271208.2(NEB):c.6507G>A (p.Lys2169=)	rs267598923
NM_001271208.2(NEB):c.914A>G (p.Asp305Gly)	rs36105240
NM_001271208.2(NEB):c.9363T>G (p.Pro3121=)	rs6709886

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