Related gene-specific medical variations for Gene (Select 221472) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3094603	NM_173558.4(FGD2):c.1523G>A (p.Arg508Gln)	FGD2, LOC126859665 (R508Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2530031	NM_173558.4(FGD2):c.1565T>C (p.Leu522Pro)	FGD2, LOC126859665 (L522P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2399875	NM_173558.4(FGD2):c.1520A>G (p.Asn507Ser)	FGD2, LOC126859665 (N507S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 783459	NM_173558.4(FGD2):c.1590G>A (p.Arg530=)	FGD2, LOC126859665	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 769681	NM_173558.4(FGD2):c.1506C>T (p.Asp502=)	FGD2, LOC126859665	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 161831	NM_173558.4(FGD2):c.882+3A>C	FGD2	Single nucleotide variant (intron variant)	Malignant tumor of prostate	GUncertain significance

ClinVar