ClinVar Miner

Submissions for variant NM_000094.3(COL7A1):c.8305-20G>C (rs17256786)

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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 RCV000250667 SCV000302266 benign not specified criteria provided, single submitter clinical testing
Invitae RCV001513412 SCV001721028 benign not provided 2020-12-03 criteria provided, single submitter clinical testing

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