ClinVar Miner

Submissions for variant NM_018062.4(FANCL):c.822-4T>G

dbSNP: rs2104795280
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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 RCV002154898 SCV002336712 likely benign Fanconi anemia 2021-03-10 criteria provided, single submitter clinical testing

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