ClinVar Miner

Submissions for variant NM_002421.3(MMP1):c.-1673G=

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV000018649 SCV000038932 pathogenic Pulmonary disease, chronic obstructive, rate of decline of lung function in 2008-02-01 no assertion criteria provided literature only
OMIM RCV000018650 SCV000038933 risk factor Epidermolysis bullosa dystrophica, autosomal recessive, modifier of 2008-02-01 no assertion criteria provided literature only
OMIM RCV000018651 SCV000038934 pathogenic Preterm premature rupture of membranes 2008-02-01 no assertion criteria provided literature only

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