ClinVar Miner

Submissions for variant NM_020937.4(FANCM):c.240C>T (p.Gly80=)

dbSNP: rs1254073558
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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 RCV001322307 SCV001513172 likely benign Fanconi anemia 2024-04-16 criteria provided, single submitter clinical testing

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