"GenomeConnect - Brain Gene Registry"[submitter] AND "STAG1"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 440451	NM_005862.3(STAG1):c.2936A>G (p.Lys979Arg)	STAG1 (K979R)	Single nucleotide variant (missense variant)	Intellectual disability, autosomal dominant 47	GLikely pathogenic
Select item 1679663	NM_005862.3(STAG1):c.1189G>C (p.Val397Leu)	STAG1 (V397L)	Single nucleotide variant (missense variant)	Intellectual disability, autosomal dominant 47 +1 more	GConflicting classifications of pathogenicity