ClinVar Miner

Submissions for variant NM_001379286.1(ZNF423):c.1194G>A (p.Pro398=)

gnomAD frequency: 0.00494  dbSNP: rs61747467
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ClinVar version:
Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000243884 SCV000312329 benign not specified criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000530780 SCV000652400 benign Nephronophthisis 14 2024-01-20 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV000530780 SCV002514227 benign Nephronophthisis 14 2021-12-05 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004714593 SCV005289758 benign not provided criteria provided, single submitter not provided

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