"GeneDx"[submitter] AND "CERNA3"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 60362	GRCh38/hg38 8q12.1(chr8:55423413-58836753)x1	BPNT2, CERNA3 +105 more	Copy number loss	See cases	GPathogenic
Select item 1294444	NC_000008.11:g.56074681C>G	CERNA3, RPS20	Single nucleotide variant (non-coding transcript variant)	not provided	GBenign
Select item 1267784	NC_000008.11:g.56074699G>C	CERNA3, RPS20	Single nucleotide variant (non-coding transcript variant)	not provided	GBenign
Select item 1294449	NC_000008.11:g.56074746C>G	CERNA3, RPS20	Single nucleotide variant (non-coding transcript variant)	not provided	GBenign
Select item 1241647	NC_000008.11:g.56074770G>C	CERNA3, RPS20	Single nucleotide variant (non-coding transcript variant)	not provided	GBenign
Select item 1286759	NC_000008.11:g.56074788T>A	CERNA3, RPS20	Single nucleotide variant (non-coding transcript variant)	not provided	GBenign
Select item 1257223	NC_000008.11:g.56074789C>T	CERNA3, RPS20	Single nucleotide variant (non-coding transcript variant)	not provided	GBenign
Select item 1264120	NC_000008.11:g.56074895C>T	CERNA3, RPS20	Single nucleotide variant	not provided	GBenign

ClinVar