ClinVar Miner

Submissions for variant NM_153240.5(NPHP3):c.1525-12T>G

gnomAD frequency: 0.00001  dbSNP: rs1939606303
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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 RCV003748914 SCV004558880 likely benign Nephronophthisis 2022-12-21 criteria provided, single submitter clinical testing

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