List of variants reported as not provided for nemaline myopathy 2 by GenomeConnect, ClinGen

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_001164508.2(NEB):c.3986A>C (p.Asp1329Ala)	rs115986826	0.00095
NM_001164508.2(NEB):c.18410C>T (p.Thr6137Met)	rs201462794	0.00019
NM_001164508.2(NEB):c.194C>T (p.Pro65Leu)	rs375909006	0.00009
NM_001164508.2(NEB):c.5087T>C (p.Ile1696Thr)	rs937014596	0.00001

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