"SIB Swiss Institute of Bioinformatics"[submitter] AND "SETBP1"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1031	NM_015559.3(SETBP1):c.2612T>C (p.Ile871Thr)	SETBP1 (I871T)	Single nucleotide variant (missense variant)	SETBP1-related condition +5 more	GConflicting classifications of pathogenicity
Select item 159873	NM_015559.3(SETBP1):c.3388C>A (p.Pro1130Thr)	SETBP1 (P1130T)	Single nucleotide variant (missense variant)	not provided +2 more	GBenign