List of variants in gene SH3BP2 reported as likely pathogenic for cherubism

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_001122681.2(SH3BP2):c.1252C>A (p.Pro418Thr)	rs757336022
NM_001122681.2(SH3BP2):c.1253C>T (p.Pro418Leu)	rs121909146
NM_001122681.2(SH3BP2):c.1259G>C (p.Gly420Ala)	rs28938171

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