ClinVar Miner

Submissions for variant NM_000558.5(HBA1):c.-37A>C

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Department of Medical Genomics, Royal Prince Alfred Hospital RCV003444050 SCV004171037 uncertain significance alpha Thalassemia 2023-11-23 no assertion criteria provided clinical testing

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