List of variants in gene MMP2 reported as pathogenic for not provided

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 9

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HGVS	dbSNP	gnomAD frequency
NC_000016.9:g.(?_55513392)_(55539354_?)del
NM_004530.6(MMP2):c.1081G>T (p.Glu361Ter)	rs1962353336
NM_004530.6(MMP2):c.1160G>A (p.Trp387Ter)
NM_004530.6(MMP2):c.1287del (p.Asn430fs)	rs794727916
NM_004530.6(MMP2):c.1743_1744dup (p.Ile582fs)	rs2543539243
NM_004530.6(MMP2):c.265del (p.Asp90fs)	rs794727275
NM_004530.6(MMP2):c.481C>T (p.Arg161Ter)
NM_004530.6(MMP2):c.732C>A (p.Tyr244Ter)	rs121912954
NM_004530.6(MMP2):c.865C>T (p.Gln289Ter)	rs1962317500

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