"GeneDx"[submitter] AND "FCN3"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 59928	GRCh38/hg38 1p36.11-35.3(chr1:26807012-27685191)x1	AHDC1, CD164L2 +98 more	Copy number loss	See cases	GPathogenic
Select item 58058	GRCh38/hg38 1p36.11-35.2(chr1:26963045-32279045)x3	ADGRB2, AHDC1 +348 more	Copy number gain	See cases	GPathogenic
Select item 1305261	NM_003665.4(FCN3):c.596G>A (p.Arg199His)	FCN3 (R188H +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance

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