"GeneDx"[submitter] AND "PREX2"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 60364	GRCh38/hg38 8q12.3-21.11(chr8:62230636-73227786)x1	ADHFE1, ARFGEF1 +228 more	Copy number loss	See cases	GPathogenic
Select item 1274701	NM_024870.4(PREX2):c.1195C>A (p.Arg399=)	PREX2	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1253695	NM_024870.4(PREX2):c.1200G>A (p.Lys400=)	PREX2	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1283008	NM_024870.4(PREX2):c.1239-7C>G	PREX2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1288091	NM_024870.4(PREX2):c.2385C>T (p.Phe795=)	PREX2	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1274446	NM_024870.4(PREX2):c.3882G>A (p.Lys1294=)	PREX2	Single nucleotide variant (synonymous variant)	not provided	GBenign

ClinVar