ClinVar Miner

Submissions for variant NM_020821.3(VPS13C):c.806_807insCAGA (p.Arg269fs)

dbSNP: rs879253853
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Brain and Spine Institute, INSERM RCV000236948 SCV000262817 pathogenic Parkinson disease 2015-11-16 criteria provided, single submitter research

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