"Genome Diagnostics Laboratory, University Medical Center Utrecht"[sub - ClinVar - NCBI

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Items: 5

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 95376	NM_001379110.1(SLC9A6):c.1460+4A>G	SLC9A6	Single nucleotide variant (intron variant)	not specified +2 more	GBenign
Select item 139206	NM_001379110.1(SLC9A6):c.1582-3C>T	SLC9A6	Single nucleotide variant (intron variant)	Christianson syndrome	GBenign FDA Recognized database
Select item 139207	NM_001379110.1(SLC9A6):c.1637G>A (p.Arg546Gln)	SLC9A6 (R568Q +4 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases +3 more	GBenign/Likely benign
Select item 139208	NM_001379110.1(SLC9A6):c.1662-4G>A	SLC9A6	Single nucleotide variant (intron variant)	Inborn genetic diseases +3 more	GBenign
Select item 139209	NM_001379110.1(SLC9A6):c.1689C>T (p.Ser563=)	SLC9A6	Single nucleotide variant (synonymous variant)	not specified +3 more	GBenign/Likely benign

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