List of variants in gene FGF10 reported as likely benign for polydactyly-syndactyly-triphalangism

Minimum submission review status:		Collection method:
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: 3

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HGVS	dbSNP	gnomAD frequency
NM_004465.1(FGF10):c.*5A>T	rs111763965	0.01295
NM_004465.2(FGF10):c.620A>C (p.His207Pro)	rs147715509	0.00152
NM_004465.2(FGF10):c.64T>C (p.Cys22Arg)

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