List of variants reported as uncertain significance for bone benign neoplasm by St. Jude Molecular Pathology, St. Jude Children's Research Hospital

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Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_016169.4(SUFU):c.839G>A (p.Arg280Gln)	rs145704867	0.00014
NM_000368.5(TSC1):c.1231C>A (p.Leu411Ile)	rs397514840	0.00003
NM_000264.5(PTCH1):c.203G>A (p.Gly68Glu)	rs757430199	0.00001
NM_000368.5(TSC1):c.1355G>C (p.Gly452Ala)	rs371093730	0.00001
NM_001042492.3(NF1):c.4836G>A (p.Arg1612=)	rs1555533268	0.00001
NM_000264.5(PTCH1):c.113G>A (p.Gly38Glu)	rs143494325

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