ClinVar Miner

Submissions for variant NM_020937.4(FANCM):c.1396+10A>G

gnomAD frequency: 0.00009  dbSNP: rs371211104
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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 RCV000536435 SCV000626351 likely benign Fanconi anemia 2024-01-05 criteria provided, single submitter clinical testing
PreventionGenetics, part of Exact Sciences RCV004537897 SCV004717142 likely benign FANCM-related disorder 2020-12-29 no assertion criteria provided clinical testing This variant is classified as likely benign based on ACMG/AMP sequence variant interpretation guidelines (Richards et al. 2015 PMID: 25741868, with internal and published modifications).

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