"Genetics Department, University Hospital of Toulouse"[submitter] AND - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 427852	NM_012186.3(FOXE3):c.232G>A (p.Ala78Thr)	FOXE3, LINC01389 (A78T)	Single nucleotide variant (missense variant)	Congenital primary aphakia +3 more	GConflicting classifications of pathogenicity
Select item 427853	NM_012186.3(FOXE3):c.310C>T (p.Arg104Cys)	FOXE3, LINC01389 (R104C)	Single nucleotide variant (missense variant)	Anterior segment dysgenesis +1 more	GConflicting classifications of pathogenicity