ClinVar Miner

Submissions for variant NM_153240.5(NPHP3):c.903A>G (p.Arg301=)

gnomAD frequency: 0.00001  dbSNP: rs375395871
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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 RCV001323685 SCV001514610 likely benign Nephronophthisis 2022-08-23 criteria provided, single submitter clinical testing

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