ClinVar Miner

Submissions for variant NM_001357.5(DHX9):c.3488A>G (p.Lys1163Arg)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Undiagnosed Diseases Network, NIH RCV004545847 SCV003932636 uncertain significance DHX9-related disorder 2022-11-22 no assertion criteria provided clinical testing

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