ClinVar Miner

Submissions for variant NM_153240.5(NPHP3):c.2475+19T>A

dbSNP: rs1031031326
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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 RCV003587114 SCV004279713 likely benign Nephronophthisis 2023-07-03 criteria provided, single submitter clinical testing

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