List of variants reported as likely benign for Nemaline Myopathy, Recessive by Illumina Laboratory Services, Illumina

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Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_000363.5(TNNI3):c.373-10=	rs7252610	0.99999
NM_003283.6(TNNT1):c.-20A>G	rs9636153	0.84878
NM_003283.6(TNNT1):c.33-8G>A	rs76630067	0.04332
NM_001164508.2(NEB):c.264_265del	rs59509952	0.02726

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