ClinVar Miner

Submissions for variant NC_000017.11:g.45982995A>G

Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Institute of Human Genetics, University of Wuerzburg RCV003229506 SCV003926511 uncertain significance Parkinsonian disorder no assertion criteria provided clinical testing

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