ClinVar Miner

Submissions for variant NM_001379286.1(ZNF423):c.1194G>T (p.Pro398=)

dbSNP: rs61747467
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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 RCV001459079 SCV001662914 likely benign Nephronophthisis 14 2024-08-04 criteria provided, single submitter clinical testing

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