ClinVar Miner

Submissions for variant NM_015102.5(NPHP4):c.279+47T>G

gnomAD frequency: 0.01612  dbSNP: rs115690090
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
Eurofins Ntd Llc (ga) RCV000596251 SCV000700432 benign not specified 2017-02-10 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004714086 SCV005280508 benign not provided criteria provided, single submitter not provided

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