ClinVar Miner

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

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Gene type:
ClinVar version:
Total variants: 68
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HGVS dbSNP gnomAD frequency
NM_004530.6(MMP2):c.1473-66T>G rs243838 0.80395
NM_004530.6(MMP2):c.1149T>C (p.Asp383=) rs243849 0.80135
NM_004530.6(MMP2):c.154-1406A>C rs837547 0.77930
NM_004530.6(MMP2):c.154-113T>A rs857403 0.77792
NM_004530.6(MMP2):c.380+185G>A rs865094 0.76260
NM_004530.6(MMP2):c.1472+93G>A rs243843 0.72547
NM_004530.6(MMP2):c.1880-60C>G rs243832 0.50074
NM_004530.6(MMP2):c.154-1621T>C rs837546 0.48314
NM_004530.6(MMP2):c.1880-274C>T rs243833 0.47597
NM_004530.6(MMP2):c.833-255G>C rs2241145 0.46229
NM_004530.6(MMP2):c.1770-4A>G rs243834 0.44856
NM_004530.6(MMP2):c.1770-69C>T rs243835 0.44827
NM_004530.6(MMP2):c.380+115A>G rs1477017 0.37701
NM_004530.6(MMP2):c.154-54G>A rs1030868 0.37668
NM_004530.6(MMP2):c.154-348G>A rs8055959 0.37103
NM_004530.6(MMP2):c.*260A>C rs7201 0.36871
NM_004530.6(MMP2):c.1806C>T (p.Phe602=) rs14070 0.36635
NM_004530.6(MMP2):c.1472+217T>C rs243842 0.36484
NM_004530.6(MMP2):c.1337-194G>A rs243844 0.36444
NM_004530.6(MMP2):c.1337-44A>T rs11640428 0.36066
NM_004530.6(MMP2):c.1380G>A (p.Thr460=) rs2287074 0.36020
NM_004530.6(MMP2):c.1180+262T>C rs243847 0.35552
NM_004530.6(MMP2):c.1769+98T>C rs2287076 0.35063
NM_004530.6(MMP2):c.530-334A>G rs11646643 0.31311
NM_004530.6(MMP2):c.1473-76G>T rs171498 0.30691
NM_004530.6(MMP2):c.154-1228G>A rs1030870 0.29807
NM_004530.6(MMP2):c.154-1200T>C rs1030869 0.26755
NM_004530.6(MMP2):c.678G>C (p.Gly226=) rs1132896 0.26147
NM_004530.6(MMP2):c.154-1126A>T rs708269 0.24098
NM_004530.6(MMP2):c.153+79C>T rs243862 0.18209
NM_004530.6(MMP2):c.-61G>C rs2287073 0.10610
NM_004530.6(MMP2):c.529+182C>T rs11076101 0.08384
NM_004530.6(MMP2):c.1842C>G (p.Pro614=) rs11541998 0.07433
NM_004530.6(MMP2):c.750C>T (p.Thr250=) rs1053605 0.05988
NM_004530.3(MMP2):c.-448G>T rs17859829 0.05654
NM_004530.6(MMP2):c.1180+46G>C rs12599775 0.02836
NM_004530.6(MMP2):c.832+12C>T rs17859889 0.02723
NM_004530.6(MMP2):c.1180+153A>G rs243848 0.02688
NM_004530.6(MMP2):c.1098C>T (p.Ala366=) rs16955236 0.02278
NM_004530.6(MMP2):c.*159T>C rs17860019 0.01829
NM_004530.6(MMP2):c.*1062C>T rs2052264 0.01706
NM_004530.6(MMP2):c.1007-18G>A rs17242473 0.01246
NM_004530.6(MMP2):c.1337-7T>C rs17859942 0.01222
NM_004530.6(MMP2):c.1066C>T (p.Leu356=) rs41513346 0.01084
NM_004530.6(MMP2):c.1340C>T (p.Ala447Val) rs17859943 0.00942
NM_004530.6(MMP2):c.1227G>A (p.Met409Ile) rs59727333 0.00635
NM_004530.6(MMP2):c.1861G>C (p.Val621Leu) rs16955280 0.00152
NM_004530.6(MMP2):c.1548C>T (p.Leu516=) rs41521545 0.00118
NM_004530.6(MMP2):c.1569A>G (p.Val523=) rs115179673 0.00111
NM_004530.6(MMP2):c.759C>T (p.Ser253=) rs148801200 0.00108
NM_004530.6(MMP2):c.496G>A (p.Glu166Lys) rs147947052 0.00081
NM_004530.6(MMP2):c.*93C>T rs112159982 0.00071
NM_004530.6(MMP2):c.658+10G>A rs201653184 0.00069
NM_004530.6(MMP2):c.154-11A>G rs371842908 0.00066
NM_004530.6(MMP2):c.*111G>A rs111489165 0.00063
NM_004530.6(MMP2):c.1609+16C>A rs17859973 0.00026
NM_004530.6(MMP2):c.1769+10G>A rs201956873 0.00024
NM_004530.6(MMP2):c.51C>T (p.Leu17=) rs41503347 0.00022
NM_004530.6(MMP2):c.1336+10C>T rs375047862 0.00020
NM_004530.6(MMP2):c.1779G>A (p.Glu593=) rs202060835 0.00006
NM_004530.6(MMP2):c.1007-12C>G rs140079276
NM_004530.6(MMP2):c.1007-13C>T
NM_004530.6(MMP2):c.1254G>A (p.Gly418=)
NM_004530.6(MMP2):c.1336+45G>C rs243846
NM_004530.6(MMP2):c.1499G>A (p.Arg500His) rs28730814
NM_004530.6(MMP2):c.832+143T>G rs111278338
NM_004530.6(MMP2):c.832+18T>A
NM_004530.6(MMP2):c.833-221G>A rs2241146

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