List of variants in gene SMARCB1 reported as benign for SMARCB1-related schwannomatosis

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

Total variants: 14

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HGVS	dbSNP	gnomAD frequency
NM_003073.5(SMARCB1):c.897G>A (p.Ser299=)	rs2229354	0.10948
NM_003073.5(SMARCB1):c.-117C>T	rs11090285	0.08005
NM_003073.5(SMARCB1):c.362+7C>T	rs34746244	0.00815
NM_003073.5(SMARCB1):c.438A>G (p.Pro146=)	rs35105793	0.00536
NM_003073.5(SMARCB1):c.-31C>T	rs34276473	0.00535
NM_003073.5(SMARCB1):c.-115C>T	rs551328283	0.00242
NM_003073.5(SMARCB1):c.628+13C>T	rs184021903	0.00235
NM_003073.5(SMARCB1):c.-184G>A	rs563943196	0.00165
NM_003073.5(SMARCB1):c.*293C>T	rs754865420	0.00051
NM_003073.5(SMARCB1):c.*33T>G	rs11541580	0.00034
NM_003073.5(SMARCB1):c.1A>G (p.Met1Val)	rs367768260	0.00020
NM_003073.5(SMARCB1):c.-17C>T	rs372777519	0.00006
NM_003073.5(SMARCB1):c.1032C>T (p.Gly344=)	rs149451748	0.00004
NM_003073.5(SMARCB1):c.978C>T (p.Tyr326=)	rs187488637	0.00003

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