ClinVar Miner

Submissions for variant NM_001128178.3(NPHP1):c.329+18C>T

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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 RCV003825714 SCV004623209 likely benign Nephronophthisis 2024-02-02 criteria provided, single submitter clinical testing

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