ClinVar Miner

Submissions for variant NM_015102.5(NPHP4):c.3576G>T (p.Arg1192=)

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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 RCV002617069 SCV002955887 likely benign Nephronophthisis 2022-10-26 criteria provided, single submitter clinical testing

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