"Department of Rehabilitation Medicine, Incheon St. Mary’s Hospital, C - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 635184	NM_001083961.2(WDR62):c.883-4_890del	WDR62	Deletion (splice acceptor variant)	Microcephaly 2, primary, autosomal recessive, with or without cortical malformations	GLikely pathogenic
Select item 635183	NM_001083961.2(WDR62):c.1684C>G (p.His562Asp)	WDR62 (H562D)	Single nucleotide variant (missense variant)	Microcephaly 2, primary, autosomal recessive, with or without cortical malformations	GLikely pathogenic