ClinVar Miner

Submissions for variant NM_000037.4(ANK1):c.3763C>T (p.Arg1255Cys)

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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 RCV003141410 SCV003818579 uncertain significance Hereditary spherocytosis type 1 2023-07-23 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV004809971 SCV005434722 uncertain significance not provided 2024-10-01 criteria provided, single submitter clinical testing ANK1: PM2, BP1

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