ClinVar Miner

Submissions for variant NM_000136.3(FANCC):c.166-7T>C

gnomAD frequency: 0.00027  dbSNP: rs369052148
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000205280 SCV000259298 likely benign Fanconi anemia 2024-01-16 criteria provided, single submitter clinical testing
Preventiongenetics, part of Exact Sciences RCV000249999 SCV000302518 likely benign not specified criteria provided, single submitter clinical testing
Mendelics RCV000988223 SCV001137860 likely benign Fanconi anemia complementation group A 2019-05-28 criteria provided, single submitter clinical testing
GeneDx RCV001651065 SCV001865440 benign not provided 2015-03-03 criteria provided, single submitter clinical testing

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