"STYXL1-related disorder"[Disease/phenotype] AND "PreventionGenetics, - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3042540	NM_001317785.2(STYXL1):c.931C>G (p.Pro311Ala)	STYXL1 (P173A +2 more)	Single nucleotide variant (missense variant +2 more)	STYXL1-related disorder	GBenign
Select item 3060119	NM_001317785.2(STYXL1):c.489C>T (p.Ile163=)	STYXL1	Single nucleotide variant (synonymous variant +1 more)	STYXL1-related disorder	GBenign
Select item 3041363	NM_001317785.2(STYXL1):c.89A>G (p.Tyr30Cys)	STYXL1 (Y30C)	Single nucleotide variant (missense variant +2 more)	STYXL1-related disorder	GLikely benign

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