"Eurofins Ntd Llc (ga)"[submitter] AND "FGD4"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 215968	NM_001370298.3(FGD4):c.666A>T (p.Ala222=)	FGD4	Single nucleotide variant (synonymous variant +3 more)	Charcot-Marie-Tooth disease +5 more	GConflicting classifications of pathogenicity
Select item 197374	NM_001370298.3(FGD4):c.846C>G (p.Asp282Glu)	FGD4 (D145E +3 more)	Single nucleotide variant (missense variant +3 more)	Charcot-Marie-Tooth disease +4 more	GBenign
Select item 476946	NM_001370298.3(FGD4):c.1296C>T (p.Phe432=)	FGD4	Single nucleotide variant (synonymous variant +1 more)	Inborn genetic diseases +4 more	GBenign/Likely benign
Select item 194280	NM_001370298.3(FGD4):c.1971C>T (p.Ile657=)	FGD4	Single nucleotide variant (synonymous variant)	Inborn genetic diseases +5 more	GBenign/Likely benign
Select item 194438	NM_001370298.3(FGD4):c.2070C>G (p.Ala690=)	FGD4	Single nucleotide variant (synonymous variant)	Charcot-Marie-Tooth disease +5 more	GBenign/Likely benign
Select item 188396	NM_001370298.3(FGD4):c.2122C>A (p.Pro708Thr)	FGD4 (P571T +6 more)	Single nucleotide variant (missense variant)	Charcot-Marie-Tooth disease +5 more	GBenign/Likely benign
Select item 188373	NM_001370298.3(FGD4):c.2560G>A (p.Val854Met)	FGD4 (V717M +5 more)	Single nucleotide variant (missense variant)	Charcot-Marie-Tooth disease type 4H +4 more	GConflicting classifications of pathogenicity

ClinVar