ClinVar Miner

Submissions for variant NM_000037.4(ANK1):c.*385del

dbSNP: rs112209933
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000306529 SCV000473815 likely benign Spherocytosis, Dominant 2016-06-14 criteria provided, single submitter clinical testing
GeneDx RCV001692058 SCV001907579 benign not provided 2021-06-18 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV002253393 SCV002524952 benign Hereditary spherocytosis type 1 2021-12-05 criteria provided, single submitter clinical testing

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