ClinVar Miner

List of variants reported as uncertain significance for childhood-onset nemaline myopathy by HudsonAlpha Institute for Biotechnology, HudsonAlpha Institute for Biotechnology

Included ClinVar conditions (18):

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_001164508.2(NEB):c.61G>A (p.Glu21Lys)	rs199907781	0.00013
NM_152263.4(TPM3):c.329C>T (p.Ala110Val)	rs1558052023

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