ClinVar Miner

Submissions for variant NM_000136.3(FANCC):c.1533+9C>T

dbSNP: rs863224323
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Counsyl RCV000670456 SCV000795310 likely benign Fanconi anemia complementation group C 2017-11-02 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001458184 SCV001662000 likely benign Fanconi anemia 2015-10-30 criteria provided, single submitter clinical testing

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