List of variants in gene MMP2 reported as likely benign by CeGaT Center for Human Genetics Tuebingen

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_004530.6(MMP2):c.759C>T (p.Ser253=)	rs148801200	0.00108
NM_004530.6(MMP2):c.96G>T (p.Ser32=)	rs146220690	0.00055
NM_004530.6(MMP2):c.51C>T (p.Leu17=)	rs41503347	0.00022
NM_004530.6(MMP2):c.1572C>T (p.Tyr524=)	rs374801798	0.00021
NM_004530.6(MMP2):c.1197C>T (p.Leu399=)	rs200082849	0.00009
NM_004530.6(MMP2):c.1659C>G (p.Pro553=)	rs747523622
NM_004530.6(MMP2):c.762T>C (p.Asp254=)

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