ClinVar Miner

Submissions for variant NM_000136.3(FANCC):c.657C>T (p.Phe219=)

dbSNP: rs2135426603
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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 RCV002166799 SCV002331998 likely benign Fanconi anemia 2021-02-23 criteria provided, single submitter clinical testing

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