ClinVar Miner

Submissions for variant NM_000037.4(ANK1):c.5372A>T (p.Asn1791Ile)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Revvity Omics, Revvity RCV003141402 SCV003818569 uncertain significance Hereditary spherocytosis type 1 2022-10-27 criteria provided, single submitter clinical testing
Diagnostic Genetics, Severance Hospital, Yonsei University College of Medicine RCV003234602 SCV003932459 uncertain significance Hemolytic anemia 2023-06-12 criteria provided, single submitter clinical testing

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