C2678194[trait identifier] AND "Revvity Omics, Revvity"[submitter] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1323617	NM_001379110.1(SLC9A6):c.886-1C>A	SLC9A6	Single nucleotide variant (splice acceptor variant)	Christianson syndrome	GPathogenic
Select item 2436077	NM_001379110.1(SLC9A6):c.1307-8C>T	SLC9A6	Single nucleotide variant (intron variant)	Christianson syndrome	GUncertain significance
Select item 1205275	NM_001379110.1(SLC9A6):c.1313G>A (p.Arg438His)	SLC9A6 (R406H +3 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 943113	NM_001379110.1(SLC9A6):c.1555G>A (p.Gly519Ser)	SLC9A6 (G519S +4 more)	Single nucleotide variant (missense variant)	Christianson syndrome	GUncertain significance
Select item 1006408	NM_001379110.1(SLC9A6):c.1765G>A (p.Glu589Lys)	SLC9A6 (E527K +4 more)	Single nucleotide variant (missense variant)	Christianson syndrome +1 more	GUncertain significance
Select item 2436078	NM_001379110.1(SLC9A6):c.1891A>G (p.Met631Val)	SLC9A6 (M569V +4 more)	Single nucleotide variant (missense variant)	Christianson syndrome	GUncertain significance

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