ClinVar Miner

Submissions for variant NM_000136.3(FANCC):c.345+19C>T

dbSNP: rs1273512627
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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 RCV003523573 SCV004369388 likely benign Fanconi anemia 2023-10-14 criteria provided, single submitter clinical testing

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