ClinVar for MedGen (Select 462027) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2579121	NM_173653.4(SLC9A9):c.1380G>T (p.Met460Ile)	SLC9A9 (M460I)	Single nucleotide variant (missense variant)	Autism, susceptibility to, 16	GUncertain significance
Select item 2431637	NM_173653.4(SLC9A9):c.119del (p.Leu40fs)	SLC9A9 (L40fs)	Deletion (frameshift variant)	Autism, susceptibility to, 16	GUncertain significance
Select item 1691277	NM_173653.4(SLC9A9):c.1268G>A (p.Arg423Gln)	SLC9A9 (R423Q)	Single nucleotide variant (missense variant)	Autism, susceptibility to, 16	GUncertain significance
Select item 996870	NM_173653.4(SLC9A9):c.1203+1G>A	SLC9A9	Single nucleotide variant (splice donor variant)	Autism, susceptibility to, 16	GUncertain significance
Select item 252794	NM_173653.4(SLC9A9):c.1486G>A (p.Asp496Asn)	SLC9A9 (D496N)	Single nucleotide variant (missense variant)	not specified +1 more	GLikely benign
Select item 2363	NM_173653.4(SLC9A9):c.1267C>T (p.Arg423Ter)	SLC9A9 (R423*)	Single nucleotide variant (nonsense)	Autism, susceptibility to, 16	Grisk factor

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