ClinVar Miner

Submissions for variant NM_001355436.2(SPTB):c.326G>A (p.Arg109His)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center RCV003991918 SCV004810310 uncertain significance Hereditary spherocytosis type 2 2024-04-04 criteria provided, single submitter clinical testing

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