List of variants reported as likely benign for cherubism by Fulgent Genetics, Fulgent Genetics

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_001122681.2(SH3BP2):c.801C>T (p.Cys267=)	rs114926004	0.01089
NM_001122681.2(SH3BP2):c.1686A>G (p.Ter562Trp)	rs190648042	0.00072
NM_001122681.2(SH3BP2):c.1549-12C>A	rs202005559	0.00054
NM_001122681.2(SH3BP2):c.247C>A (p.Arg83=)	rs139626310	0.00005

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