"Genomic Diagnostic Laboratory, Division of Genomic Diagnostics, Child - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 252726	NM_020066.5(FMN2):c.1481C>G (p.Pro494Arg)	FMN2 (P494R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 218763	NM_020066.5(FMN2):c.1966C>T (p.Arg656Cys)	FMN2 (R660C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 218764	NM_020066.5(FMN2):c.2828C>T (p.Pro943Leu)	FMN2 (P947L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 218765	NM_020066.5(FMN2):c.2840C>T (p.Pro947Leu)	FMN2 (P951L +1 more)	Single nucleotide variant (missense variant +1 more)	FMN2-related disorder +2 more	GBenign/Likely benign
Select item 218766	NM_020066.5(FMN2):c.2897T>C (p.Leu966Pro)	FMN2 (L970P +1 more)	Single nucleotide variant (missense variant +1 more)	FMN2-related disorder +2 more	GConflicting classifications of pathogenicity
Select item 218767	NM_020066.5(FMN2):c.3413C>T (p.Ala1138Val)	FMN2 (A1142V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified +1 more	GConflicting classifications of pathogenicity

ClinVar