"PreventionGenetics, part of Exact Sciences"[submitter] AND "TBX19"[ge - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3034929	NM_005149.3(TBX19):c.-3C>T	TBX19	Single nucleotide variant (5 prime UTR variant)	TBX19-related disorder	GLikely benign
Select item 293454	NM_005149.3(TBX19):c.105C>T (p.Asp35=)	TBX19	Single nucleotide variant (synonymous variant)	not provided +2 more	GBenign
Select item 293456	NM_005149.3(TBX19):c.204-3T>C	TBX19	Single nucleotide variant (intron variant)	not specified +3 more	GConflicting classifications of pathogenicity
Select item 1598565	NM_005149.3(TBX19):c.369C>T (p.Tyr123=)	TBX19	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 5443	NM_005149.3(TBX19):c.782del (p.Asn261fs)	TBX19 (N261fs)	Deletion (frameshift variant)	TBX19-related disorder +2 more	GPathogenic
Select item 2057988	NM_005149.3(TBX19):c.1053-7T>C	TBX19	Single nucleotide variant (intron variant)	not provided +1 more	GBenign/Likely benign

ClinVar