"PreventionGenetics, part of Exact Sciences"[submitter] AND "FGF3"[gen - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3048764	NM_005247.4(FGF3):c.651G>A (p.Pro217=)	FGF3	Single nucleotide variant (synonymous variant)	FGF3-related disorder	GLikely benign
Select item 259689	NM_005247.4(FGF3):c.420G>A (p.Thr140=)	FGF3	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 259688	NM_005247.4(FGF3):c.408G>A (p.Thr136=)	FGF3	Single nucleotide variant (synonymous variant)	not specified +1 more	GBenign
Select item 3046749	NM_005247.4(FGF3):c.333C>T (p.Tyr111=)	FGF3	Single nucleotide variant (synonymous variant)	FGF3-related disorder	GLikely benign
Select item 259687	NM_005247.4(FGF3):c.325-5C>T	FGF3	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 13838	NM_005247.4(FGF3):c.310C>T (p.Arg104Ter)	FGF3 (R104*)	Single nucleotide variant (nonsense)	not provided +2 more	GPathogenic/Likely pathogenic
Select item 38385	NM_005247.4(FGF3):c.283C>T (p.Arg95Trp)	FGF3 (R95W)	Single nucleotide variant (missense variant)	not provided +1 more	GPathogenic/Likely pathogenic
Select item 259690	NM_005247.4(FGF3):c.69G>T (p.Ala23=)	FGF3, LOC109115964	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign

ClinVar