"Baylor Genetics"[submitter] AND "SLC9A6"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1030062	NM_001379110.1(SLC9A6):c.-57+50G>C	LOC130068746, SLC9A6 (A9P)	Single nucleotide variant (missense variant +1 more)	Christianson syndrome	GUncertain significance
Select item 1032437	NM_001379110.1(SLC9A6):c.1080+17A>G	SLC9A6	Single nucleotide variant (intron variant)	Christianson syndrome	GConflicting classifications of pathogenicity
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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