"PreventionGenetics, part of Exact Sciences"[submitter] AND "SLC9A3-AS - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3044618	NM_004174.4(SLC9A3):c.2382T>C (p.Ser794=)	SLC9A3, SLC9A3-AS1	Single nucleotide variant (synonymous variant)	SLC9A3-related disorder	GLikely benign
Select item 1546948	NM_004174.4(SLC9A3):c.2223C>G (p.Thr741=)	SLC9A3, SLC9A3-AS1	Single nucleotide variant (synonymous variant)	SLC9A3-related disorder +1 more	GLikely benign
Select item 1601494	NM_004174.4(SLC9A3):c.1816C>T (p.Arg606Trp)	SLC9A3, SLC9A3-AS1 (R597W +1 more)	Single nucleotide variant (missense variant)	SLC9A3-related disorder +1 more	GBenign/Likely benign
Select item 1166328	NM_004174.4(SLC9A3):c.1811G>A (p.Arg604Gln)	SLC9A3, SLC9A3-AS1 (R595Q +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign
Select item 791026	NM_004174.4(SLC9A3):c.1728G>A (p.Ser576=)	SLC9A3, SLC9A3-AS1	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 1541334	NM_004174.4(SLC9A3):c.1530C>T (p.Phe510=)	SLC9A3, SLC9A3-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	SLC9A3-related disorder +1 more	GLikely benign

ClinVar