"GeneDx"[submitter] AND "RNF41"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 152934	GRCh38/hg38 12q13.13-13.3(chr12:53420606-56202942)x3	PMEL, PPP1R1A +219 more	Copy number gain	See cases	GPathogenic
Select item 1245767	NM_005785.4(RNF41):c.602+193T>C	RNF41	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1265710	NM_005785.4(RNF41):c.499-206C>A	RNF41	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1266669	NM_005785.4(RNF41):c.91-66_91-65del	RNF41	Microsatellite (intron variant)	not provided	GBenign
Select item 1278348	NM_005785.4(RNF41):c.91-121G>A	RNF41	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1232459	NM_005785.4(RNF41):c.91-137A>G	RNF41	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1234461	NM_005785.4(RNF41):c.-23-73G>A	RNF41	Single nucleotide variant (intron variant)	not provided	GBenign

ClinVar