ClinVar Miner

Submissions for variant GRCh38/hg38 16q24.3(chr16:89764796-89811592)x1

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Institute of Medical Genetics and Applied Genomics, University Hospital Tübingen RCV003236702 SCV003935188 pathogenic Fanconi anemia complementation group A 2023-06-26 criteria provided, single submitter clinical testing

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