ClinVar for MedGen (Select 863911) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2435915	NM_001199251.3(SGO1):c.1178C>G (p.Thr393Arg)	SGO1, SGO1-AS1 (T393R)	Single nucleotide variant (non-coding transcript variant +2 more)	Chronic atrial and intestinal dysrhythmia	GUncertain significance
Select item 162627	NM_001199251.3(SGO1):c.67A>G (p.Lys23Glu)	SGO1, SGO1-AS1 (K23E)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GPathogenic