"PreventionGenetics, part of Exact Sciences"[submitter] AND "SLC9A6"[g - ClinVar - NCBI

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Items: 14

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 378617	NM_001379110.1(SLC9A6):c.-60T>C	LOC130068746, SLC9A6	Single nucleotide variant (5 prime UTR variant +2 more)	SLC9A6-related disorder +1 more	GLikely benign
Select item 657261	NM_001379110.1(SLC9A6):c.-57+32C>T	LOC130068746, SLC9A6 (R3W)	Single nucleotide variant (missense variant +1 more)	Christianson syndrome +1 more	GUncertain significance
Select item 159933	NM_001379110.1(SLC9A6):c.-57+50G>T	LOC130068746, SLC9A6 (A9S)	Single nucleotide variant (missense variant +1 more)	Christianson syndrome	GBenign FDA Recognized database
Select item 940098	NM_001379110.1(SLC9A6):c.-56-21C>A	SLC9A6 (P27H)	Single nucleotide variant (missense variant +1 more)	Christianson syndrome +1 more	GUncertain significance
Select item 207247	NM_001379110.1(SLC9A6):c.-9G>T	SLC9A6 (A50S)	Single nucleotide variant (missense variant +1 more)	Christianson syndrome	GLikely benign FDA Recognized database
Select item 3031257	NM_001379110.1(SLC9A6):c.403T>C (p.Leu135=)	SLC9A6	Single nucleotide variant (synonymous variant)	SLC9A6-related disorder	GLikely benign
Select item 139200	NM_001379110.1(SLC9A6):c.474T>C (p.Ser158=)	SLC9A6	Single nucleotide variant (synonymous variant)	SLC9A6-related disorder +3 more	GBenign/Likely benign
Select item 656614	NM_001379110.1(SLC9A6):c.483A>G (p.Ala161=)	SLC9A6	Single nucleotide variant (synonymous variant)	Christianson syndrome +1 more	GLikely benign
Select item 139201	NM_001379110.1(SLC9A6):c.744-6C>T	SLC9A6	Single nucleotide variant (intron variant)	not specified +1 more	GBenign
Select item 2145570	NM_001379110.1(SLC9A6):c.1059G>A (p.Glu353=)	SLC9A6	Single nucleotide variant (synonymous variant)	Christianson syndrome +1 more	GBenign/Likely benign
Select item 469632	NM_001379110.1(SLC9A6):c.1083G>A (p.Leu361=)	SLC9A6	Single nucleotide variant (synonymous variant)	Christianson syndrome	GBenign FDA Recognized database
Select item 95375	NM_001379110.1(SLC9A6):c.1306+8G>A	SLC9A6	Single nucleotide variant (intron variant)	Christianson syndrome +2 more	GBenign/Likely benign
Select item 95376	NM_001379110.1(SLC9A6):c.1460+4A>G	SLC9A6	Single nucleotide variant (intron variant)	not specified +3 more	GBenign
Select item 139209	NM_001379110.1(SLC9A6):c.1689C>T (p.Ser563=)	SLC9A6	Single nucleotide variant (synonymous variant)	Christianson syndrome +2 more	GBenign/Likely benign