ClinVar Miner

Submissions for variant NM_020937.4(FANCM):c.177C>T (p.Val59=)

dbSNP: rs2139100946
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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 RCV001432990 SCV001635773 likely benign Fanconi anemia 2019-11-26 criteria provided, single submitter clinical testing

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