ClinVar Miner

Submissions for variant NM_145239.3(PRRT2):c.-65-15CTC[2]

dbSNP: rs1555502536
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV002464268 SCV000721199 likely benign not provided 2022-11-23 criteria provided, single submitter clinical testing See Variant Classification Assertion Criteria.

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