"GeneDx"[submitter] AND "PRM2"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 58594	GRCh38/hg38 16p13.3-13.13(chr16:23141-11296695)x3	ABAT, ABCA3 +822 more	Copy number gain	See cases	GPathogenic
Select item 1262511	NC_000016.10:g.11275571C>T	PRM2	Single nucleotide variant	not provided	GBenign
Select item 1289745	NM_002762.4(PRM2):c.272-61C>A	PRM2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1272249	NM_002762.4(PRM2):c.271+27G>C	PRM2 (A100P)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 1296631	NC_000016.10:g.11276596C>T	PRM2	Single nucleotide variant	not provided	GBenign
Select item 1250057	NC_000016.10:g.11276741C>G	PRM2	Single nucleotide variant	not provided	GBenign
Select item 1258512	NC_000016.10:g.11276759G>A	PRM2	Single nucleotide variant	not provided	GBenign
Select item 253820	GRCh37/hg19 16p13.13(chr16:11173868-11681288)x3	PRM2, PRM3 +6 more	Copy number gain	See cases	GUncertain significance

ClinVar