ClinVar Miner

Submissions for variant NM_015102.5(NPHP4):c.993-184C>T

gnomAD frequency: 0.52481  dbSNP: rs10779677
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
GeneDx RCV001710916 SCV001938571 benign not provided 2021-05-13 criteria provided, single submitter clinical testing

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