ClinVar Miner

Submissions for variant NM_001379286.1(ZNF423):c.100+13G>A

gnomAD frequency: 0.00463  dbSNP: rs143660882
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000254382 SCV000312351 benign not specified criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001520550 SCV001729672 benign Nephronophthisis 14 2024-01-25 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001520550 SCV002514232 benign Nephronophthisis 14 2021-12-05 criteria provided, single submitter clinical testing

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