ClinVar Miner

Submissions for variant NM_000311.5(PRNP):c.180T>C (p.Pro60=)

dbSNP: rs1386720703
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Undiagnosed Diseases Network, NIH RCV000549562 SCV000622169 uncertain significance Spongiform encephalopathy with neuropsychiatric features 2016-06-26 criteria provided, single submitter clinical testing

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