Related gene-specific medical variations for Gene (Select 51434) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3067985	NM_016238.3(ANAPC7):c.493del (p.Cys165fs)	ANAPC7 (C165fs +2 more)	Deletion (frameshift variant +1 more)	Ferguson-Bonni neurodevelopmental syndrome	GUncertain significance
Select item 2442207	NM_016238.3(ANAPC7):c.137T>C (p.Leu46Ser)	ANAPC7 (L46S +1 more)	Single nucleotide variant (missense variant +1 more)	Ferguson-Bonni neurodevelopmental syndrome	GUncertain significance