ClinVar Miner

Submissions for variant NM_014956.5(CEP164):c.552+9G>A

gnomAD frequency: 0.00002  dbSNP: rs1278586123
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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 RCV002109428 SCV002398857 likely benign Nephronophthisis 15 2023-08-04 criteria provided, single submitter clinical testing

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