List of variants reported as uncertain significance for nemaline myopathy 2 by Broad Center for Mendelian Genomics, Broad Institute of MIT and Harvard

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_001164508.2(NEB):c.19102-10_19102-4del	rs1577576425
NM_001164508.2(NEB):c.20122G>A (p.Val6708Ile)
NM_001164508.2(NEB):c.24115-151C>A	rs1575076895
NM_001164508.2(NEB):c.7235A>G (p.Tyr2412Cys)	rs1575122611

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