ClinVar Miner

Submissions for variant NM_153240.5(NPHP3):c.1275+12del

dbSNP: rs2107990515
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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 RCV002198595 SCV002487222 likely benign Nephronophthisis 2022-07-26 criteria provided, single submitter clinical testing

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