ClinVar Miner

Submissions for variant NM_024798.3(SNX22):c.*2294G>A (rs121434559)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV000018434 SCV000038716 pathogenic Osteogenesis imperfecta type 9 2009-10-01 no assertion criteria provided literature only
Osteogenesis Imperfecta Variant Database (PPIB) RCV000024534 SCV000045838 not provided not provided 2011-02-17 no assertion provided curation

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