List of variants reported as uncertain significance for cherubism by Fulgent Genetics, Fulgent Genetics

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_001122681.2(SH3BP2):c.724del (p.His242fs)	rs747250901	0.00011
NM_001122681.2(SH3BP2):c.428+1G>C	rs769264475	0.00001
NM_001122681.2(SH3BP2):c.760T>C (p.Ser254Pro)	rs1211847666	0.00001
NM_001122681.2(SH3BP2):c.1654C>T (p.Arg552Trp)	rs151048521
NM_001122681.2(SH3BP2):c.993_994del (p.Cys331_Asp332delinsTer)	rs1171967366

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