ClinVar for MedGen (Select 333392) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 160345	NM_003868.2(FGF16):c.275_293dup	FGF16	Duplication	not provided	GLikely pathogenic
Select item 66060	NM_003868.3(FGF16):c.470C>A (p.Ser157Ter)	FGF16 (S157*)	Single nucleotide variant (nonsense)	Syndactyly type 8	GPathogenic
Select item 66059	NM_003868.3(FGF16):c.535C>T (p.Arg179Ter)	FGF16 (R179*)	Single nucleotide variant (nonsense)	Syndactyly type 8	GPathogenic

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