ClinVar for OMIM (Select 300577) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1033110	NM_144969.3(ZDHHC15):c.599G>A (p.Trp200Ter)	ZDHHC15 (W200* +1 more)	Single nucleotide variant (nonsense)	Intellectual disability, X-linked 91	GUncertain significance
Select item 625797	GRCh37/hg19 Xq13.3(chrX:74641546-74744601)	ZDHHC15	Copy number gain	Intellectual disability, X-linked 91	GPathogenic