ClinVar Miner

Submissions for variant NM_000136.3(FANCC):c.-44G>A

dbSNP: rs2136102852
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001438263 SCV001641135 likely benign Fanconi anemia 2019-05-15 criteria provided, single submitter clinical testing

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