ClinVar for MedGen (Select 322874) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1720	NM_152709.5(STOX1):c.1824A>C (p.Glu608Asp)	STOX1 (E608D)	Single nucleotide variant (missense variant +1 more)	not specified	GBenign
Select item 1719	NM_152709.5(STOX1):c.457T>C (p.Tyr153His)	STOX1 (Y153H)	Single nucleotide variant (missense variant)	Preeclampsia/eclampsia 4	Grisk factor