ClinVar Miner

Submissions for variant NM_020937.4(FANCM):c.2373C>T (p.Thr791=)

dbSNP: rs2139241090
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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 RCV001459084 SCV001662919 likely benign Fanconi anemia 2020-02-04 criteria provided, single submitter clinical testing
Quest Diagnostics Nichols Institute San Juan Capistrano RCV003478844 SCV004218741 likely benign not provided 2023-02-20 criteria provided, single submitter clinical testing

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