ClinVar Miner

Submissions for variant NM_000311.5(PRNP):c.246A>G (p.Gly82=) (rs62643364)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Clinical Services Laboratory,Illumina RCV000340924 SCV000434225 benign Genetic prion diseases 2016-06-14 criteria provided, single submitter clinical testing
Invitae RCV000644591 SCV000766291 benign Huntington disease-like 1 2017-11-04 criteria provided, single submitter clinical testing

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