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

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 58453	GRCh38/hg38 6q25.2-27(chr6:154118058-170602152)x1	ACAT2, AFDN +549 more	Copy number loss	See cases	GPathogenic
Select item 59548	GRCh38/hg38 6q26(chr6:161289959-162789916)x3	LOC105378098, LOC121132714 +13 more	Copy number gain	See cases	GUncertain significance
Select item 1220094	NM_004562.3(PRKN):c.7+111G>A	PACRG, PRKN	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1300469	NM_004562.3(PRKN):c.7+5G>A	PACRG, PRKN	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 356022	NM_004562.3(PRKN):c.-30T>C	PACRG, PRKN	Single nucleotide variant (5 prime UTR variant +1 more)	Autosomal recessive juvenile Parkinson disease 2 +1 more	GLikely benign
Select item 1270795	NC_000006.12:g.162727992T>C	PACRG, PRKN	Single nucleotide variant (5 prime UTR variant +1 more)	not provided	GBenign
Select item 152770	GRCh38/hg38 6q26(chr6:162916759-163095219)x3	LOC126859872, PACRG +1 more	Copy number gain	See cases	GUncertain significance

ClinVar