ClinVar Miner

Submissions for variant NM_020937.4(FANCM):c.682-7T>C

gnomAD frequency: 0.00001  dbSNP: rs1012042292
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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 RCV000869188 SCV001010596 likely benign Fanconi anemia 2025-01-23 criteria provided, single submitter clinical testing
Quest Diagnostics Nichols Institute San Juan Capistrano RCV003478544 SCV004218844 likely benign not provided 2023-09-16 criteria provided, single submitter clinical testing

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