C1268935[trait identifier] AND "Baylor Genetics"[submitter] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1031635	NM_139027.6(ADAMTS13):c.427A>G (p.Ile143Val)	ADAMTS13 (I143V)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 632074	NM_139027.6(ADAMTS13):c.559G>C (p.Asp187His)	ADAMTS13 (D187H)	Single nucleotide variant (missense variant +1 more)	not specified +2 more	GConflicting classifications of pathogenicity
Select item 914641	NM_139027.6(ADAMTS13):c.1156C>T (p.Arg386Cys)	ADAMTS13 (R386C +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 1031632	NM_139027.6(ADAMTS13):c.1810G>A (p.Val604Ile)	ADAMTS13 (V573I +1 more)	Single nucleotide variant (missense variant +1 more)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 68815	NM_139027.6(ADAMTS13):c.3178C>T (p.Arg1060Trp)	ADAMTS13 (R1060W +1 more)	Single nucleotide variant (missense variant +1 more)	ADAMTS13-related condition +3 more	GPathogenic/Likely pathogenic
Select item 2441914	NM_139027.6(ADAMTS13):c.3292A>G (p.Thr1098Ala)	ADAMTS13 (T1067A +1 more)	Single nucleotide variant (missense variant +1 more)	Upshaw-Schulman syndrome	GUncertain significance

ClinVar