ClinVar Miner

Submissions for variant NM_018062.4(FANCL):c.96+18G>A

dbSNP: rs1694510595
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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 RCV003866993 SCV004671129 likely benign Fanconi anemia 2023-05-13 criteria provided, single submitter clinical testing

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