ClinVar Miner

Submissions for variant NM_014956.5(CEP164):c.1410-2A>G

gnomAD frequency: 0.00054  dbSNP: rs200074826
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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 RCV001523166 SCV001732836 benign Nephronophthisis 15 2023-04-24 criteria provided, single submitter clinical testing

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