C3554499[trait identifier] AND "Genomic Medicine Lab, University of Ca - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 816879	NM_022095.4(ZNF335):c.3589C>T (p.Gln1197Ter)	ZNF335 (Q1197*)	Single nucleotide variant (nonsense)	Microcephalic primordial dwarfism due to ZNF335 deficiency	GUncertain significance
Select item 816878	NM_022095.4(ZNF335):c.1856G>A (p.Arg619His)	ZNF335 (R619H)	Single nucleotide variant (missense variant)	Microcephalic primordial dwarfism due to ZNF335 deficiency +1 more	GUncertain significance