ClinVar Miner

Submissions for variant NM_015102.5(NPHP4):c.3316-177G>A

gnomAD frequency: 0.05253  dbSNP: rs78598342
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001715315 SCV001940483 benign not provided 2021-05-18 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001715315 SCV005286763 benign not provided criteria provided, single submitter not provided

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