"GeneDx"[submitter] AND "TXN2"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 57629	GRCh38/hg38 22q12.3-13.1(chr22:35333993-38900177)x1	ANKRD54, APOL1 +293 more	Copy number loss	See cases	GPathogenic
Select item 59058	GRCh38/hg38 22q12.3(chr22:35753347-36593973)x3	APOL1, APOL2 +43 more	Copy number gain	See cases	GUncertain significance
Select item 1222057	NM_012473.4(TXN2):c.*173AG[1]	TXN2	Microsatellite (3 prime UTR variant)	not provided	GBenign
Select item 1271118	NM_012473.4(TXN2):c.388-99C>A	TXN2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1280669	NM_012473.4(TXN2):c.387+30A>C	TXN2	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 1231242	NM_012473.4(TXN2):c.1-174T>C	TXN2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1294498	NC_000022.11:g.36481648_36481649insGA	TXN2	Insertion (genic upstream transcript variant)	not provided	GBenign
Select item 253617	GRCh37/hg19 22q12.3-13.33(chr22:35728929-51220961)x3	A4GALT, ACO2 +223 more	Copy number gain	See cases	GPathogenic
Select item 253509	GRCh37/hg19 22q11.1-13.33(chr22:16054691-51237518)x3	A4GALT, ACO2 +438 more	Copy number gain	See cases	GPathogenic

ClinVar