ClinVar Miner

Submissions for variant NM_000136.3(FANCC):c.1534-18C>T

gnomAD frequency: 0.00001  dbSNP: rs1289718209
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Mendelics RCV000988193 SCV001137830 likely benign Fanconi anemia complementation group A 2019-05-28 criteria provided, single submitter clinical testing
GeneDx RCV001712842 SCV001939494 benign not provided 2015-08-03 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002488078 SCV002794977 likely benign Fanconi anemia complementation group C 2021-08-25 criteria provided, single submitter clinical testing
Invitae RCV002549704 SCV003439272 likely benign Fanconi anemia 2023-06-23 criteria provided, single submitter clinical testing

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