ClinVar Miner

Submissions for variant NM_014956.5(CEP164):c.3999A>G (p.Gln1333=)

dbSNP: rs201718007
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001516590 SCV001724889 benign Nephronophthisis 15 2023-07-28 criteria provided, single submitter clinical testing

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