ClinVar Miner

Submissions for variant NM_001379286.1(ZNF423):c.3516+14A>G

gnomAD frequency: 0.00041  dbSNP: rs201606291
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 RCV001432741 SCV001635520 likely benign Nephronophthisis 14 2024-12-04 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004706141 SCV005216396 likely benign not provided criteria provided, single submitter not provided

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