ClinVar Miner

Submissions for variant NM_000135.4(FANCA):c.3393_3395delinsA (p.Ala1132fs)

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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 RCV003460176 SCV004196647 likely pathogenic Fanconi anemia complementation group A 2021-11-17 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV003460176 SCV005642627 likely pathogenic Fanconi anemia complementation group A 2024-04-05 criteria provided, single submitter clinical testing

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