ClinVar Miner

List of variants reported as benign for nemaline myopathy 2 by Fulgent Genetics, Fulgent Genetics

Included ClinVar conditions (2):

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.5971C>T (p.His1991Tyr)	rs75807392	0.04908
NM_001164508.2(NEB):c.19056G>T (p.Thr6352=)	rs115631125	0.00354

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