ClinVar Miner

Submissions for variant NM_020937.4(FANCM):c.924G>A (p.Leu308=)

dbSNP: rs756513033
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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 RCV001396999 SCV001598737 likely benign Fanconi anemia 2023-10-22 criteria provided, single submitter clinical testing
Quest Diagnostics Nichols Institute San Juan Capistrano RCV003478813 SCV004218851 likely benign not provided 2022-09-09 criteria provided, single submitter clinical testing

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