"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "MMP9"[gene - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 708035	NM_004994.3(MMP9):c.113A>G (p.Asn38Ser)	MMP9 (N38S)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign
Select item 773609	NM_004994.3(MMP9):c.559C>T (p.Leu187Phe)	MMP9 (L187F)	Single nucleotide variant (missense variant)	Metaphyseal anadysplasia 2 +2 more	GBenign/Likely benign
Select item 1675858	NM_004994.3(MMP9):c.1743C>T (p.Phe581=)	MMP9, SLC12A5-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GLikely benign

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ClinVar