ClinVar Miner

Submissions for variant NM_001018115.3(FANCD2):c.1656+7G>A

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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 RCV003822921 SCV004620412 likely benign Fanconi anemia 2023-08-06 criteria provided, single submitter clinical testing

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