ClinVar Miner

Submissions for variant NM_012179.4(FBXO7):c.1144+1G>T (rs730880272)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Institute of Human Genetics,Klinikum rechts der Isar RCV000005079 SCV000680236 pathogenic Parkinson disease 15 2017-11-16 criteria provided, single submitter clinical testing
OMIM RCV000005079 SCV000025255 pathogenic Parkinson disease 15 2009-01-20 no assertion criteria provided literature only

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