ClinVar Miner

Submissions for variant NM_001379286.1(ZNF423):c.912G>A (p.Gln304=)

gnomAD frequency: 0.00004  dbSNP: rs147427609
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002209707 SCV002369090 likely benign Nephronophthisis 14 2024-10-29 criteria provided, single submitter clinical testing

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