ClinVar Miner

Submissions for variant NM_000136.3(FANCC):c.1330-8T>C

dbSNP: rs864622221
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000206510 SCV000259757 likely benign Fanconi anemia 2023-04-28 criteria provided, single submitter clinical testing
Counsyl RCV000666867 SCV000791231 uncertain significance Fanconi anemia complementation group C 2017-05-05 criteria provided, single submitter clinical testing

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