Related gene-specific medical variations for Gene (Select 9508) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3065425	NM_014243.3(ADAMTS3):c.2878C>T (p.Pro960Ser)	ADAMTS3 (P960S)	Single nucleotide variant (missense variant)	Hennekam lymphangiectasia-lymphedema syndrome 3	GUncertain significance
Select item 3064779	NM_014243.3(ADAMTS3):c.3104G>A (p.Arg1035Gln)	ADAMTS3 (R1035Q)	Single nucleotide variant (missense variant)	Hennekam lymphangiectasia-lymphedema syndrome 3	GUncertain significance
Select item 980093	GRCh37/hg19 4q13.3(chr4:73222936-73389169)x1	ADAMTS3	Copy number loss	not provided	GLikely benign
Select item 814568	GRCh37/hg19 4q13.3(chr4:73184648-73813059)x3	ADAMTS3	Copy number gain	not provided	GUncertain significance
Select item 443509	GRCh37/hg19 4q13.3(chr4:73184648-73812869)x3	ADAMTS3	Copy number gain	See cases	GUncertain significance
Select item 161671	NM_014243.3(ADAMTS3):c.64G>T (p.Gly22Ter)	ADAMTS3 (G22*)	Single nucleotide variant (nonsense)	Malignant tumor of prostate	GUncertain significance

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