"Clinical Genetics, Academic Medical Center"[submitter] AND "LINC01389 - ClinVar - NCBI

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Items: 5

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 287849	NM_012186.3(FOXE3):c.16G>A (p.Asp6Asn)	FOXE3, LINC01389 (D6N)	Single nucleotide variant (missense variant)	not provided +4 more	GBenign/Likely benign
Select item 385608	NM_012186.3(FOXE3):c.234G>A (p.Ala78=)	FOXE3, LINC01389	Single nucleotide variant (synonymous variant)	Familial thoracic aortic aneurysm and aortic dissection +6 more	GBenign/Likely benign
Select item 260211	NM_012186.3(FOXE3):c.423G>A (p.Lys141=)	FOXE3, LINC01389	Single nucleotide variant (synonymous variant)	not provided +4 more	GBenign
Select item 468250	NM_012186.3(FOXE3):c.587G>C (p.Gly196Ala)	FOXE3, LINC01389 (G196A)	Single nucleotide variant (missense variant)	Familial thoracic aortic aneurysm and aortic dissection +5 more	GBenign/Likely benign
Select item 777909	NM_012186.3(FOXE3):c.828C>G (p.Pro276=)	FOXE3, LINC01389	Single nucleotide variant (synonymous variant)	not provided +4 more	GBenign/Likely benign

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