"GeneDx"[submitter] AND "FZD2"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 58696	GRCh38/hg38 17q12-21.31(chr17:39199873-45629579)x3	LOC130060786, LOC130060787 +633 more	Copy number gain	See cases	GPathogenic
Select item 59586	GRCh38/hg38 17q21.31(chr17:43570878-44762377)x1	ADAM11, ASB16 +104 more	Copy number loss	See cases	GPathogenic
Select item 1282177	NC_000017.11:g.44557317G>C	FZD2	Single nucleotide variant	not provided	GBenign
Select item 1288439	NM_001466.4(FZD2):c.660T>C (p.Asp220=)	FZD2	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2444708	NM_001466.4(FZD2):c.809T>C (p.Met270Thr)	FZD2 (M270T)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 784745	NM_001466.4(FZD2):c.909C>T (p.Arg303=)	FZD2	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2497890	NM_001466.4(FZD2):c.1163T>G (p.Leu388Arg)	FZD2 (L388R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1279907	NM_001466.4(FZD2):c.*300G>T	FZD2	Single nucleotide variant (3 prime UTR variant)	not provided	GBenign

ClinVar