ClinVar Miner

Submissions for variant NM_001379286.1(ZNF423):c.1062G>A (p.Arg354=)

gnomAD frequency: 0.00001  dbSNP: rs1400739360
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002183300 SCV002423038 likely benign Nephronophthisis 14 2022-05-21 criteria provided, single submitter clinical testing

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