"Pathology and Clinical Laboratory Medicine, King Fahad Medical City"[ - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 982114	NM_001124759.5(FRG2C):c.179-112A>G	FRG2C	Single nucleotide variant (intron variant)	not specified	GBenign
Select item 982115	NM_001124759.5(FRG2C):c.278A>G (p.Gln93Arg)	FRG2C (Q93R)	Single nucleotide variant (missense variant)	not specified	GBenign
Select item 982116	NM_001124759.5(FRG2C):c.317T>G (p.Ile106Ser)	FRG2C (I106S)	Single nucleotide variant (missense variant)	not specified	GBenign
Select item 982117	NM_001124759.5(FRG2C):c.334+93C>T	FRG2C	Single nucleotide variant (intron variant)	not specified	GBenign
Select item 982118	NM_001124759.5(FRG2C):c.334+114A>G	FRG2C	Single nucleotide variant (intron variant)	not specified	GBenign
Select item 982119	NM_001124759.5(FRG2C):c.359A>G (p.Asn120Ser)	FRG2C (N120S)	Single nucleotide variant (missense variant)	not specified	GBenign
Select item 982120	NM_001124759.5(FRG2C):c.497A>G (p.Glu166Gly)	FRG2C (E166G)	Single nucleotide variant (missense variant)	not specified	GBenign

ClinVar