ClinVar Miner

Submissions for variant NM_000037.4(ANK1):c.5164del (p.Gln1722fs)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Revvity Omics, Revvity RCV003489311 SCV004238448 likely pathogenic Hereditary spherocytosis type 1 2023-05-15 criteria provided, single submitter clinical testing

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