ClinVar Miner

Submissions for variant NM_000135.4(FANCA):c.2594_2595del (p.Ile865fs)

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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 RCV003460145 SCV004196034 likely pathogenic Fanconi anemia complementation group A 2023-09-08 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV003460145 SCV005644475 likely pathogenic Fanconi anemia complementation group A 2024-01-23 criteria provided, single submitter clinical testing

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