"GeneDx"[submitter] AND "TCF3"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 60066	GRCh38/hg38 19p13.3(chr19:945098-1972299)x1	LOC130062906, LOC130062907 +222 more	Copy number loss	See cases	GPathogenic
Select item 59081	GRCh38/hg38 19p13.3(chr19:1565575-4108128)x3	ABHD17A, ADAT3 +362 more	Copy number gain	See cases	GPathogenic
Select item 1169440	NM_003200.5(TCF3):c.1308C>T (p.Gly436=)	TCF3	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 1167431	NM_003200.5(TCF3):c.1302A>G (p.Ser434=)	TCF3	Single nucleotide variant (synonymous variant)	not specified +1 more	GBenign
Select item 1169720	NM_003200.5(TCF3):c.1293C>T (p.Gly431=)	TCF3	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1167884	NM_003200.5(TCF3):c.1291G>A (p.Gly431Ser)	TCF3 (G430S +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 253623	GRCh37/hg19 19p13.3(chr19:277373-2555164)x3	ABCA7, ABHD17A +87 more	Copy number gain	See cases	GPathogenic

ClinVar