C4693572[trait identifier] AND "Victorian Clinical Genetics Services, - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1804913	NM_014875.3(KIF14):c.4353+7T>A	KIF14	Single nucleotide variant (intron variant)	Microcephaly 20, primary, autosomal recessive	GUncertain significance
Select item 1805932	NM_014875.3(KIF14):c.1979+2C>T	KIF14	Single nucleotide variant (splice donor variant)	Microcephaly 20, primary, autosomal recessive	GUncertain significance