ClinVar Miner

Submissions for variant NM_020937.4(FANCM):c.508+19A>G

dbSNP: rs2503037555
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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 RCV003070561 SCV003476987 likely benign Fanconi anemia 2022-09-14 criteria provided, single submitter clinical testing

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