ClinVar Miner

Submissions for variant NM_005523.6(HOXA11):c.380A>G (p.Tyr127Cys)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV005234291 SCV005879124 uncertain significance Radioulnar synostosis with amegakaryocytic thrombocytopenia 1 2024-05-01 criteria provided, single submitter clinical testing

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