ClinVar Miner

Submissions for variant NM_020937.4(FANCM):c.4387-16del

dbSNP: rs1371203135
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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 RCV002717399 SCV003010844 benign Fanconi anemia 2024-12-18 criteria provided, single submitter clinical testing

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