ClinVar Miner

Submissions for variant NM_001379286.1(ZNF423):c.40+33082T>A

gnomAD frequency: 0.00006  dbSNP: rs556089941
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002157013 SCV002332058 likely benign Nephronophthisis 14 2024-05-02 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002157013 SCV002795644 likely benign Nephronophthisis 14 2022-01-07 criteria provided, single submitter clinical testing

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