List of variants reported as uncertain significance for schwannoma by Illumina Laboratory Services, Illumina

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Total variants: 18

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HGVS	dbSNP	gnomAD frequency
NM_003073.5(SMARCB1):c.*159C>G	rs1022324232	0.00055
NM_003073.5(SMARCB1):c.*113C>T	rs886057286	0.00008
NM_003073.5(SMARCB1):c.-148T>C	rs886057283	0.00003
NM_003073.5(SMARCB1):c.-149C>T	rs886057282	0.00002
NM_003073.5(SMARCB1):c.309C>T (p.Asn103=)	rs145695677	0.00002
NM_003073.5(SMARCB1):c.607G>A (p.Ala203Thr)	rs762962010	0.00002
NM_003073.5(SMARCB1):c.*279G>A	rs886057287	0.00001
NM_003073.5(SMARCB1):c.-83C>T	rs1374186002	0.00001
NM_003073.5(SMARCB1):c.*100C>G	rs1363655817
NM_003073.5(SMARCB1):c.12_14dup	rs779825754
NM_003073.5(SMARCB1):c.*197A>C	rs1306414841
NM_003073.5(SMARCB1):c.*307A>G	rs2030874248
NM_003073.5(SMARCB1):c.-107A>G	rs886057284
NM_003073.5(SMARCB1):c.-157G>A	rs886057281
NM_003073.5(SMARCB1):c.1118+8T>C	rs2030796889
NM_003073.5(SMARCB1):c.633G>A (p.Lys211=)	rs1930218305
NM_003073.5(SMARCB1):c.723C>T (p.Ile241=)	rs752910574
NM_003073.5(SMARCB1):c.987-4G>C	rs745773662

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