C4552002[trait identifier] AND "Center for Genomics, Ann and Robert H. - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 787569	NM_030957.4(ADAMTS10):c.2403+4A>G	ADAMTS10	Single nucleotide variant (intron variant)	Weill-Marchesani syndrome +3 more	GBenign/Likely benign
Select item 2500013	NM_030957.4(ADAMTS10):c.2361C>G (p.Ser787Arg)	ADAMTS10 (S274R +1 more)	Single nucleotide variant (missense variant)	Weill-Marchesani syndrome 1	GUncertain significance
Select item 625880	NM_030957.4(ADAMTS10):c.1920G>A (p.Ser640=)	ADAMTS10	Single nucleotide variant (synonymous variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 2500008	NM_030957.4(ADAMTS10):c.1659G>C (p.Trp553Cys)	ADAMTS10 (G44A +1 more)	Single nucleotide variant (missense variant)	Weill-Marchesani syndrome 1	GUncertain significance
Select item 2500012	NM_030957.4(ADAMTS10):c.1084+6C>T	ADAMTS10	Single nucleotide variant (intron variant)	Weill-Marchesani syndrome 1	GUncertain significance
Select item 625881	NM_030957.4(ADAMTS10):c.641C>G (p.Pro214Arg)	ADAMTS10 (P214R)	Single nucleotide variant (missense variant)	Weill-Marchesani syndrome 1	GUncertain significance
Select item 625879	NM_030957.4(ADAMTS10):c.350C>T (p.Ala117Val)	ADAMTS10 (A117V)	Single nucleotide variant (missense variant)	not provided +2 more	GConflicting classifications of pathogenicity

ClinVar