ClinVar Miner

Submissions for variant NM_000037.4(ANK1):c.3841del (p.Arg1281fs)

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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 RCV003489296 SCV004238431 likely pathogenic Hereditary spherocytosis type 1 2023-03-27 criteria provided, single submitter clinical testing

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