C4540493[trait identifier] AND "Undiagnosed Diseases Network, NIH"[sub - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2691775	NM_006295.3(VARS1):c.3288G>T (p.Glu1096Asp)	VARS1 (E1096D)	Single nucleotide variant (missense variant)	Neurodevelopmental disorder with microcephaly, seizures, and cortical atrophy	GUncertain significance
Select item 2691776	NM_006295.3(VARS1):c.2590_2592delinsTGA (p.Ser864Ter)	VARS1 (S864*)	Indel (nonsense)	Neurodevelopmental disorder with microcephaly, seizures, and cortical atrophy	GLikely pathogenic