ClinVar Miner

Submissions for variant NM_001379286.1(ZNF423):c.69G>A (p.Ser23=)

dbSNP: rs375314927
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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 RCV002119737 SCV002398550 likely benign Nephronophthisis 14 2023-07-16 criteria provided, single submitter clinical testing

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