"Baylor Genetics"[submitter] AND "CLIC2"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1029305	NM_001289.6(CLIC2):c.103C>T (p.Arg35Cys)	CLIC2 (R35C)	Single nucleotide variant (missense variant)	X-linked intellectual disability-cardiomegaly-congestive heart failure syndrome	GUncertain significance
Select item 625803	GRCh37/hg19 Xq28(chrX:153761240-155227607)	BRCC3, CLIC2 +22 more	Copy number loss	not provided	GLikely pathogenic
Select item 625671	GRCh37/hg19 Xq26.3-28(chrX:134975270-155233945)	ABCD1, ADGRG4 +160 more	Copy number gain	not provided	GPathogenic

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