ClinVar Miner

Submissions for variant NM_000311.3(PRNP):c.204_227del24 (p.Pro84_Gln91del) (rs193922906)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000644588 SCV000766288 likely benign not provided 2018-12-14 criteria provided, single submitter clinical testing
GeneReviews RCV000055681 SCV000086596 non-pathogenic Genetic prion diseases 2008-12-18 no assertion criteria provided curation Converted during submission to Benign.

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