ClinVar Miner

Submissions for variant NM_018062.4(FANCL):c.472-15A>G

dbSNP: rs374750427
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002171543 SCV002477984 likely benign Fanconi anemia 2023-08-28 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002486982 SCV002803789 likely benign Fanconi anemia complementation group L 2021-10-06 criteria provided, single submitter clinical testing

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