ClinVar Miner

Submissions for variant NM_138295.5(PKD1L1):c.399-195C>T

gnomAD frequency: 0.09459  dbSNP: rs12702399
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 RCV001684706 SCV001901791 benign not provided 2021-06-20 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001684706 SCV005264970 benign not provided criteria provided, single submitter not provided

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