ClinVar Miner

Submissions for variant NM_020821.3(VPS13C):c.10414+1G>A

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genomic Medicine Center of Excellence, King Faisal Specialist Hospital and Research Centre RCV003991764 SCV004809967 likely pathogenic Autosomal recessive early-onset Parkinson disease 23 2024-04-04 criteria provided, single submitter clinical testing

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