ClinVar Miner

Submissions for variant NM_001018115.3(FANCD2):c.426T>A (p.Ile142=)

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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 RCV003635759 SCV004484024 likely benign Fanconi anemia 2023-02-26 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV005030214 SCV005656858 uncertain significance Fanconi anemia complementation group D2 2024-05-07 criteria provided, single submitter clinical testing

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