ClinVar Miner

Submissions for variant NM_015450.3(POT1):c.1505+7TGTTT[7]

dbSNP: rs66826272
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001686543 SCV001902115 benign not provided 2019-08-07 criteria provided, single submitter clinical testing
Clinical Genetics Laboratory, Department of Pathology, Netherlands Cancer Institute RCV001694162 SCV001906365 benign not specified no assertion criteria provided clinical testing
Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen RCV001694162 SCV001963565 benign not specified no assertion criteria provided clinical testing

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