C5569025[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 1333851	NM_001303256.3(MORC2):c.2119C>T (p.Arg707Trp)	MORC2 (R645W +1 more)	Single nucleotide variant (missense variant)	Charcot-Marie-Tooth disease axonal type 2Z	GUncertain significance
Select item 1333852	NM_001303256.3(MORC2):c.426+58C>T	MORC2	Single nucleotide variant (intron variant)	Charcot-Marie-Tooth disease axonal type 2Z	GUncertain significance