"GeneDx"[submitter] AND "RETREG3"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 58696	GRCh38/hg38 17q12-21.31(chr17:39199873-45629579)x3	LOC130060786, LOC130060787 +633 more	Copy number gain	See cases	GPathogenic
Select item 1290158	NC_000017.11:g.42609109G>A	RETREG3, TUBG1	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 1263791	NC_000017.11:g.42609235C>T	RETREG3, TUBG1	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 1291801	NC_000017.11:g.42609261G>A	LOC130060913, RETREG3 +1 more (R22C)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 1304893	NC_000017.11:g.42609299G>A	LOC130060913, RETREG3 +1 more (T9M)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 1296635	NC_000017.11:g.42609333G>C	LOC130060913, RETREG3 +1 more	Single nucleotide variant (5 prime UTR variant +1 more)	not provided	GBenign
Select item 672681	NM_001070.4(TUBG1):c.-403C>A	RETREG3, TUBG1 +1 more	Single nucleotide variant (5 prime UTR variant +1 more)	not provided	GBenign
Select item 1220105	NC_000017.11:g.42609350G>A	LOC130060913, RETREG3 +1 more	Single nucleotide variant (5 prime UTR variant +1 more)	not provided	GLikely benign
Select item 1189783	NC_000017.11:g.42609362G>A	LOC130060913, RETREG3 +1 more	Single nucleotide variant (5 prime UTR variant +1 more)	not provided	GLikely benign

ClinVar