ClinVar Miner

List of variants in gene combination LOC129992073, SH3BP2 reported as benign for Fibrous dysplasia of jaw

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_001122681.2(SH3BP2):c.*1656T>C	rs146752554	0.00411
NM_001122681.2(SH3BP2):c.*1679C>T	rs549256215	0.00170

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