ClinVar Miner

Submissions for variant NM_000136.3(FANCC):c.687-5G>T

dbSNP: rs767811745
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Mendelics RCV000988213 SCV001137850 likely benign Fanconi anemia complementation group A 2019-05-28 criteria provided, single submitter clinical testing

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