List of variants in gene SMARCB1 reported as likely benign for schwannoma

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

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_003073.5(SMARCB1):c.696G>A (p.Thr232=)	rs145934279	0.00029
NM_003073.5(SMARCB1):c.*15C>A	rs369400289	0.00028
NM_003073.5(SMARCB1):c.*17C>T	rs372348692	0.00009

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