List of variants reported as not provided for nemaline myopathy 2 by GenomeConnect - Invitae Patient Insights Network

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_001164508.2(NEB):c.19675G>A (p.Val6559Ile)	rs189232206	0.00021
NM_001164508.2(NEB):c.23083C>A (p.Pro7695Thr)	rs757006805	0.00006
NM_001164508.2(NEB):c.21734A>G (p.Asn7245Ser)	rs751872533	0.00001
NM_001164508.2(NEB):c.16994A>C (p.Asn5665Thr)	rs2153806253
NM_001164508.2(NEB):c.3264_3265del (p.Tyr1088_Lys1089delinsTer)	rs2099386637

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