ClinVar Miner

Submissions for variant NM_007262.5(PARK7):c.399G>C (p.Met133Ile)

dbSNP: rs398124657
Minimum review status: Collection method:
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Neurogenetic Laboratory, Oslo University Hospital RCV000082873 SCV000114936 uncertain significance Parkinson disease, late-onset 2014-01-22 no assertion criteria provided research

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