"PreventionGenetics, part of Exact Sciences"[submitter] AND "MMP9"[gen - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 707836	NM_004994.3(MMP9):c.70C>T (p.Arg24Cys)	MMP9 (R24C)	Single nucleotide variant (missense variant)	MMP9-related disorder +2 more	GBenign/Likely benign
Select item 3039334	NM_004994.3(MMP9):c.371+7C>G	MMP9	Single nucleotide variant (intron variant)	MMP9-related disorder	GLikely benign
Select item 1056493	NM_004994.3(MMP9):c.519G>A (p.Ala173=)	MMP9	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 773609	NM_004994.3(MMP9):c.559C>T (p.Leu187Phe)	MMP9 (L187F)	Single nucleotide variant (missense variant)	MMP9-related disorder +2 more	GBenign/Likely benign
Select item 782929	NM_004994.3(MMP9):c.840C>T (p.Asp280=)	MMP9	Single nucleotide variant (synonymous variant)	Metaphyseal anadysplasia 2 +2 more	GBenign
Select item 3055734	NM_004994.3(MMP9):c.1720C>A (p.Arg574=)	MMP9, SLC12A5-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	MMP9-related disorder	GLikely benign

ClinVar