ClinVar Miner

Submissions for variant NM_002739.5(PRKCG):c.-192_-178del

gnomAD frequency: 0.00229  dbSNP: rs557551763
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV003328962 SCV004035677 likely benign not provided 2022-02-09 criteria provided, single submitter clinical testing See Variant Classification Assertion Criteria.

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