C1856113[trait identifier] AND "Centogene AG - the Rare Disease Compan - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 974830	NM_014795.4(ZEB2):c.1683_1689dup (p.Asp564fs)	ZEB2 (D540fs +1 more)	Duplication (frameshift variant)	Mowat-Wilson syndrome	GLikely pathogenic
Select item 1076838	NM_014795.4(ZEB2):c.876dup (p.Tyr293fs)	ZEB2 (Y269fs +1 more)	Duplication (frameshift variant)	Mowat-Wilson syndrome	GPathogenic/Likely pathogenic
Select item 1333977	NM_014795.4(ZEB2):c.74-15372C>A	ZEB2	Single nucleotide variant (intron variant)	Mowat-Wilson syndrome	GUncertain significance

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