ClinVar Miner

Submissions for variant NM_000136.3(FANCC):c.1329+10A>G (rs977427150)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000466577 SCV000560623 likely benign not provided 2016-08-03 criteria provided, single submitter clinical testing
Mendelics RCV000988200 SCV001137837 likely benign Fanconi anemia, complementation group A 2019-05-28 criteria provided, single submitter clinical testing

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