ClinVar Miner

Submissions for variant NM_015102.5(NPHP4):c.3231+41T>C

gnomAD frequency: 0.64813  dbSNP: rs868163
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000252694 SCV000312385 benign not specified criteria provided, single submitter clinical testing
GeneDx RCV001683077 SCV001904674 benign not provided 2021-05-13 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001788129 SCV002030035 benign Nephronophthisis 4 2021-09-05 criteria provided, single submitter clinical testing

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