ClinVar Miner

Submissions for variant NM_020937.4(FANCM):c.1183+8A>G

gnomAD frequency: 0.00001  dbSNP: rs538172189
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000867600 SCV001008846 benign Fanconi anemia 2024-01-04 criteria provided, single submitter clinical testing
Quest Diagnostics Nichols Institute San Juan Capistrano RCV003478538 SCV004218709 benign not provided 2023-05-31 criteria provided, single submitter clinical testing

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