ClinVar Miner

Submissions for variant NM_000136.3(FANCC):c.1329+238C>T

gnomAD frequency: 0.00006  dbSNP: rs768988593
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Counsyl RCV000665191 SCV000789265 likely benign Fanconi anemia complementation group C 2017-01-17 criteria provided, single submitter clinical testing
Mayo Clinic Laboratories, Mayo Clinic RCV003480749 SCV004225051 uncertain significance not provided 2022-03-01 criteria provided, single submitter clinical testing PM2

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