ClinVar Miner

Submissions for variant NM_145239.3(PRRT2):c.-30T>C

gnomAD frequency: 0.00014  dbSNP: rs202072359
Minimum review status: Collection method:
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Athena Diagnostics RCV000992708 SCV001145205 likely benign not provided 2018-08-30 criteria provided, single submitter clinical testing
GeneDx RCV000992708 SCV001945641 benign not provided 2015-03-03 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV000992708 SCV005215746 likely benign not provided criteria provided, single submitter not provided

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