C4693834[trait identifier] AND "Genome-Nilou Lab"[submitter] - ClinVar - NCBI

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Items: 5

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1321850	NM_015261.3(NCAPD3):c.2892A>G (p.Val964=)	NCAPD3	Single nucleotide variant (synonymous variant)	Microcephaly 22, primary, autosomal recessive +1 more	GBenign
Select item 1321851	NM_015261.3(NCAPD3):c.1689+20A>G	NCAPD3	Single nucleotide variant (intron variant)	Microcephaly 22, primary, autosomal recessive +1 more	GBenign
Select item 1321852	NM_015261.3(NCAPD3):c.1525+18T>A	NCAPD3	Single nucleotide variant (intron variant)	Microcephaly 22, primary, autosomal recessive +1 more	GBenign
Select item 1321853	NM_015261.3(NCAPD3):c.1215+28G>A	NCAPD3	Single nucleotide variant (intron variant)	Microcephaly 22, primary, autosomal recessive +1 more	GBenign
Select item 1321854	NM_015261.3(NCAPD3):c.1090-33A>G	NCAPD3	Single nucleotide variant (intron variant)	Microcephaly 22, primary, autosomal recessive +1 more	GBenign

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