C3806730[trait identifier] AND "Center of Genomic medicine, Geneva, Un - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 397512	NM_001008537.3(NEXMIF):c.3470C>A (p.Ser1157Ter)	NEXMIF (S1157*)	Single nucleotide variant (nonsense)	X-linked intellectual disability, Cantagrel type	GPathogenic
Select item 242323	NM_001008537.3(NEXMIF):c.652C>T (p.Arg218Ter)	NEXMIF (R218*)	Single nucleotide variant (nonsense)	not provided +2 more	GPathogenic