ClinVar Miner

Submissions for variant NM_000136.3(FANCC):c.166-7T>C (rs369052148)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000205280 SCV000259298 likely benign Fanconi anemia 2019-12-31 criteria provided, single submitter clinical testing
PreventionGenetics,PreventionGenetics RCV000249999 SCV000302518 likely benign not specified criteria provided, single submitter clinical testing
Mendelics RCV000988223 SCV001137860 likely benign Fanconi anemia, complementation group A 2019-05-28 criteria provided, single submitter clinical testing

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