ClinVar Miner

Submissions for variant NM_000136.3(FANCC):c.-87G>A

gnomAD frequency: 0.00001  dbSNP: rs1051113986
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Mendelics RCV000988230 SCV001137867 likely benign Fanconi anemia complementation group A 2019-05-28 criteria provided, single submitter clinical testing
GeneDx RCV001595059 SCV001829707 benign not provided 2015-03-03 criteria provided, single submitter clinical testing

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