ClinVar Miner

Submissions for variant NM_000094.3(COL7A1):c.8620+18_8620+19insGCC (rs138595277)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics,PreventionGenetics RCV000242625 SCV000302267 likely benign not specified criteria provided, single submitter clinical testing
Invitae RCV001513337 SCV001720937 benign not provided 2020-12-05 criteria provided, single submitter clinical testing

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