ClinVar Miner

Submissions for variant NM_001379286.1(ZNF423):c.3850-9C>T

gnomAD frequency: 0.02527  dbSNP: rs78514142
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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000244059 SCV000312349 benign not specified criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000552772 SCV000652425 benign Nephronophthisis 14 2024-01-29 criteria provided, single submitter clinical testing
GeneDx RCV001683076 SCV001905462 benign not provided 2021-05-05 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV000552772 SCV002514207 benign Nephronophthisis 14 2021-12-05 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001683076 SCV005289739 benign not provided criteria provided, single submitter not provided

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