ClinVar Miner

Submissions for variant NM_001018115.3(FANCD2):c.3042T>C (p.His1014=)

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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 RCV005076533 SCV005724406 likely benign Fanconi anemia 2024-12-26 criteria provided, single submitter clinical testing

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