"Labcorp Genetics (formerly Invitae), Labcorp"[submitter] AND "PRMT2"[ - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 710386	NM_206962.4(PRMT2):c.327+7C>T	PRMT2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 748626	NM_206962.4(PRMT2):c.594T>C (p.Asp198=)	PRMT2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 779049	NM_206962.4(PRMT2):c.606C>T (p.Pro202=)	PRMT2	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 743660	NM_206962.4(PRMT2):c.831-8T>C	PRMT2	Single nucleotide variant (3 prime UTR variant +1 more)	not provided	GLikely benign
Select item 718694	NM_206962.4(PRMT2):c.1057G>A (p.Gly353Arg)	PRMT2 (G251R +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 764005	NM_206962.4(PRMT2):c.1096C>A (p.Pro366Thr)	PRMT2 (P264T +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign

ClinVar