ClinVar Miner

Submissions for variant NM_153240.5(NPHP3):c.520A>T (p.Ile174Phe)

dbSNP: rs1553775338
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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 RCV000526695 SCV000636166 uncertain significance Nephronophthisis 2021-08-27 criteria provided, single submitter clinical testing

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