List of variants in gene FGF9 reported as likely benign for bone development disease

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Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_002010.3(FGF9):c.-118_-117insC	rs1555223896	0.00456
NM_002010.3(FGF9):c.420C>T (p.Phe140=)	rs765041263	0.00006
NM_002010.3(FGF9):c.283C>G (p.Leu95Val)	rs776951218	0.00003
NM_002010.3(FGF9):c.*2497del	rs148832636

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