"New York Genome Center"[submitter] AND "NDE1"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2498201	Single allele	ABCC1, ABCC6 +57 more	Deletion	16p13.11 recurrent microdeletion syndrome	GLikely pathogenic
Select item 218495	NM_002474.3(MYH11):c.5052C>G (p.Ser1684Arg)	MYH11, NDE1 (S1691R +1 more)	Single nucleotide variant (missense variant +1 more)	not provided +3 more	GUncertain significance