ClinVar Miner

Submissions for variant NM_015102.5(NPHP4):c.1752C>T (p.Thr584=)

dbSNP: rs1443618180
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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 RCV001424950 SCV001627559 likely benign Nephronophthisis 2019-10-05 criteria provided, single submitter clinical testing

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