ClinVar Miner

Submissions for variant NM_000135.4(FANCA):c.3627-2A>G

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Baylor Genetics RCV004576529 SCV005057583 likely pathogenic Fanconi anemia complementation group A 2023-12-12 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV004576529 SCV005642603 likely pathogenic Fanconi anemia complementation group A 2024-01-28 criteria provided, single submitter clinical testing

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