ClinVar Miner

Submissions for variant NM_001386393.1(PANK2):c.1083-13dup

dbSNP: rs199905730
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001585214 SCV001818570 likely benign not provided 2020-09-01 criteria provided, single submitter clinical testing
Clinical Genetics, Academic Medical Center RCV001699822 SCV001925391 benign not specified no assertion criteria provided clinical testing
Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen RCV001585214 SCV001963238 likely benign not provided no assertion criteria provided clinical testing

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