ClinVar Miner

Submissions for variant NM_001379286.1(ZNF423):c.2697T>C (p.Cys899=)

gnomAD frequency: 0.21148  dbSNP: rs3803667
Minimum review status: Collection method:
Minimum conflict level:
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 RCV000241925 SCV000312340 benign not specified criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001518071 SCV001726705 benign Nephronophthisis 14 2024-01-31 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001518071 SCV002514216 benign Nephronophthisis 14 2021-12-05 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004715797 SCV005289750 benign not provided criteria provided, single submitter not provided

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