ClinVar Miner

Submissions for variant NM_000037.4(ANK1):c.1659G>A (p.Glu553=)

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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 RCV003741145 SCV004565312 likely benign Hereditary spherocytosis type 1 2023-07-26 criteria provided, single submitter clinical testing

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